<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
  <channel>
    <title>Medics Musings: FDA recall roundup</title>
    <link>https://www.medicsmusings.com/recalls/</link>
    <atom:link href="https://www.medicsmusings.com/feeds/recalls.xml" rel="self" type="application/rss+xml"/>
    <description>FDA drug, device and food recalls from the last 30 days, updated weekly from openFDA.</description>
    <language>en-us</language>
    <image><url>https://www.medicsmusings.com/icon-512.png</url><title>Medics Musings: FDA recall roundup</title><link>https://www.medicsmusings.com/recalls/</link></image>
    <lastBuildDate>Wed, 21 Oct 2026 12:00:00 GMT</lastBuildDate>
    <item>
      <title>Class I device recall: HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only) (Instrumentation Laboratory)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0002-2027</link>
      <guid isPermaLink="false">Z-0002-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. Recalling firm: Instrumentation Laboratory. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class I device recall: HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009800127. in vitro diagnostic (Instrumentation Laboratory)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0001-2027</link>
      <guid isPermaLink="false">Z-0001-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. Recalling firm: Instrumentation Laboratory. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class I food recall: Made Fresh brand Black Bean and Corn Salad; 5lb white plastic tub (Made Fresh Salads Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#</link>
      <guid isPermaLink="true">https://www.medicsmusings.com/recalls/#</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Products may be contaminated with Listeria monocytogenes. Recalling firm: Made Fresh Salads Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class I food recall: Deano's Pasta; Pear and Pecorino Triangoli Ravioli, 1lb.; Ingredients: Dough: Semolina (Wh (DEANO'S PASTA)</title>
      <link>https://www.medicsmusings.com/recalls/#h-0092-2027</link>
      <guid isPermaLink="false">H-0092-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Undeclared Lobster Recalling firm: DEANO'S PASTA. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II drug recall: Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 154 (Houston Rx LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#d-0041-2027</link>
      <guid isPermaLink="false">D-0041-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Lack of process control Recalling firm: Houston Rx LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II drug recall: Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured  (Teva Pharmaceuticals USA, Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#d-0038-2027</link>
      <guid isPermaLink="false">D-0038-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Presence of Foreign Tablets/Capsules Recalling firm: Teva Pharmaceuticals USA, Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II drug recall: Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: America (American Health Packaging)</title>
      <link>https://www.medicsmusings.com/recalls/#d-0042-2027</link>
      <guid isPermaLink="false">D-0042-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Presence of Foreign Tablets/Capsules Recalling firm: American Health Packaging. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II drug recall: Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactu (Zydus Pharmaceuticals (USA) Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#d-0039-2027</link>
      <guid isPermaLink="false">D-0039-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Failed Impurities/Degradation Specifications. Recalling firm: Zydus Pharmaceuticals (USA) Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II drug recall: Tirzepatide/Niacinamide 2mL vial (40 MG per Vial) Inj 20mg/2mg/mL, RX Only, Houston RX LLC (Houston Rx LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#d-0040-2027</link>
      <guid isPermaLink="false">D-0040-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Lack of assurance of sterility. Recalling firm: Houston Rx LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506. (Howmedica Osteonics Corp.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0164-2027</link>
      <guid isPermaLink="false">Z-0164-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual… Recalling firm: Howmedica Osteonics Corp.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretcher (Ferno-Washington Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0145-2027</link>
      <guid isPermaLink="false">Z-0145-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered… Recalling firm: Ferno-Washington Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. (Howmedica Osteonics Corp.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0166-2027</link>
      <guid isPermaLink="false">Z-0166-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual… Recalling firm: Howmedica Osteonics Corp.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A &amp;#38; B, Medline Produc (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0176-2027</link>
      <guid isPermaLink="false">Z-0176-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, b (Cook Incorporated)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0163-2027</link>
      <guid isPermaLink="false">Z-0163-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of this… Recalling firm: Cook Incorporated. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with a (Medtronic Sofamor Danek USA Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0138-2027</link>
      <guid isPermaLink="false">Z-0138-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed… Recalling firm: Medtronic Sofamor Danek USA Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0189-2027</link>
      <guid isPermaLink="false">Z-0189-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Discrepancy in the shelf-life of a component Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A C (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0184-2027</link>
      <guid isPermaLink="false">Z-0184-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ9 (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0178-2027</link>
      <guid isPermaLink="false">Z-0178-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0172-2027</link>
      <guid isPermaLink="false">Z-0172-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Co (Baxter Healthcare Corporation)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0151-2027</link>
      <guid isPermaLink="false">Z-0151-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients… Recalling firm: Baxter Healthcare Corporation. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513 (Beckman Coulter, Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0160-2027</link>
      <guid isPermaLink="false">Z-0160-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual… Recalling firm: Beckman Coulter, Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ9 (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0183-2027</link>
      <guid isPermaLink="false">Z-0183-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product N (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0177-2027</link>
      <guid isPermaLink="false">Z-0177-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SK (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0170-2027</link>
      <guid isPermaLink="false">Z-0170-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline p (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0174-2027</link>
      <guid isPermaLink="false">Z-0174-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with a (Medtronic Sofamor Danek USA Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0137-2027</link>
      <guid isPermaLink="false">Z-0137-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed… Recalling firm: Medtronic Sofamor Danek USA Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Generic Name: BioFire¿ Joint Infection (JI) Panel Generic Name: BioFire¿ Joint Infection ( (BioFire Diagnostics, LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0150-2027</link>
      <guid isPermaLink="false">Z-0150-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Recalling firm: BioFire Diagnostics, LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: IntelePACS, InteleConnect Portal/Tech Portal Versions PACS-5-1-1-R102, PACS-5-2-1-R93, PAC (INTELERAD MEDICAL SYSTEMS INCORPORATED)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0186-2027</link>
      <guid isPermaLink="false">Z-0186-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Following a Chromium-based web-browser, report and displayed images may not match. Recalling firm: INTELERAD MEDICAL SYSTEMS INCORPORATED. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: TS Femoral Prep Tray, Triathlon. Catalog Number: 6543-6-507. (Howmedica Osteonics Corp.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0165-2027</link>
      <guid isPermaLink="false">Z-0165-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual… Recalling firm: Howmedica Osteonics Corp.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF, Medline Product number/ (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0175-2027</link>
      <guid isPermaLink="false">Z-0175-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY PROSTATE DYKM (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0185-2027</link>
      <guid isPermaLink="false">Z-0185-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists (Radiometer Medical ApS)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0190-2027</link>
      <guid isPermaLink="false">Z-0190-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood samples no longer suitable for testing FHbF and ctBil, 2)… Recalling firm: Radiometer Medical ApS. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200 UDI (Cadwell Industries Inc)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0141-2027</link>
      <guid isPermaLink="false">Z-0141-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient, or allow an unintended electrical current to reach… Recalling firm: Cadwell Industries Inc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(1 (SI-BONE, Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0146-2027</link>
      <guid isPermaLink="false">Z-0146-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. Recalling firm: SI-BONE, Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm (In2bones USA, LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0157-2027</link>
      <guid isPermaLink="false">Z-0157-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. Recalling firm: In2bones USA, LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) SPINAL CDS, Medline Product Number/SKU CD (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0179-2027</link>
      <guid isPermaLink="false">Z-0179-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: IQ200 SPRINT, REF: 700-3322,700-3322RFB, 700-3325, 700-3326, B48997; IQ200 SELECT, REF: 70 (Beckman Coulter, Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0161-2027</link>
      <guid isPermaLink="false">Z-0161-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual… Recalling firm: Beckman Coulter, Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L (Jenavalve Technology Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0136-2027</link>
      <guid isPermaLink="false">Z-0136-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. Recalling firm: Jenavalve Technology Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115 (Steris Corporation)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0154-2027</link>
      <guid isPermaLink="false">Z-0154-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted… Recalling firm: Steris Corporation. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, REF: OPRO-101; (Microgenics Corporation)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0159-2027</link>
      <guid isPermaLink="false">Z-0159-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone (PTH) recovery, which may lead to a delay in reporting patient… Recalling firm: Microgenics Corporation. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis; Model/Catalog Number: VSWVH08 (W L Gore &amp; Associates, Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0158-2027</link>
      <guid isPermaLink="false">Z-0158-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The potential for the devices to be mislabeled with the incorrect length. Recalling firm: W L Gore &amp; Associates, Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: JenaValve Trilogy Delivery Catheter, Size 25MM REF: TRILOGY-DC-M (Jenavalve Technology Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0135-2027</link>
      <guid isPermaLink="false">Z-0135-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. Recalling firm: Jenavalve Technology Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product C (Ethicon, LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0153-2027</link>
      <guid isPermaLink="false">Z-0153-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if discovered prior to use may cause surgical delay. If… Recalling firm: Ethicon, LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF, Medline product  (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0171-2027</link>
      <guid isPermaLink="false">Z-0171-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020117 (Steris Corporation)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0156-2027</link>
      <guid isPermaLink="false">Z-0156-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted… Recalling firm: Steris Corporation. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: FORWARD Gunshot Wound Kit; Model: AFT-GSW; (INTEGRATED MEDCRAFT LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0147-2027</link>
      <guid isPermaLink="false">Z-0147-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade over time. The degradation may cause… Recalling firm: INTEGRATED MEDCRAFT LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plu (BioFire Diagnostics, LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0149-2027</link>
      <guid isPermaLink="false">Z-0149-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Recalling firm: BioFire Diagnostics, LLC. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: 1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0169-2027</link>
      <guid isPermaLink="false">Z-0169-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP C (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0182-2027</link>
      <guid isPermaLink="false">Z-0182-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT (Sarnova HC, Llc)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0144-2027</link>
      <guid isPermaLink="false">Z-0144-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. Recalling firm: Sarnova HC, Llc. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYN (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0181-2027</link>
      <guid isPermaLink="false">Z-0181-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: BD Phoenix Panel NMIC-312. Catalog Number: 449082. (Becton Dickinson &amp; Co.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0139-2027</link>
      <guid isPermaLink="false">Z-0139-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. Recalling firm: Becton Dickinson &amp; Co.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model (Healthmark Industries Co., Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0188-2027</link>
      <guid isPermaLink="false">Z-0188-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. Recalling firm: Healthmark Industries Co., Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Stan (Merit Medical Systems, Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0187-2027</link>
      <guid isPermaLink="false">Z-0187-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use. Recalling firm: Merit Medical Systems, Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/ (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0168-2027</link>
      <guid isPermaLink="false">Z-0168-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LA (Medline Industries, LP)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0180-2027</link>
      <guid isPermaLink="false">Z-0180-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Recalling firm: Medline Industries, LP. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: JenaValve Trilogy Delivery Catheter, Size 23MM REF: TRILOGY-DC-S (Jenavalve Technology Inc.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0134-2027</link>
      <guid isPermaLink="false">Z-0134-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. Recalling firm: Jenavalve Technology Inc.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: BD Phoenix Panel NMIC-306. Catalog Number: 449292. (Becton Dickinson &amp; Co.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0140-2027</link>
      <guid isPermaLink="false">Z-0140-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. Recalling firm: Becton Dickinson &amp; Co.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519. (Howmedica Osteonics Corp.)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0167-2027</link>
      <guid isPermaLink="false">Z-0167-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual… Recalling firm: Howmedica Osteonics Corp.. Status: Ongoing.</description>
    </item>
    <item>
      <title>Class II device recall: Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Ca (BioFire Diagnostics, LLC)</title>
      <link>https://www.medicsmusings.com/recalls/#z-0148-2027</link>
      <guid isPermaLink="false">Z-0148-2027</guid>
      <pubDate>Wed, 21 Oct 2026 12:00:00 GMT</pubDate>
      <description>Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results Recalling firm: BioFire Diagnostics, LLC. Status: Ongoing.</description>
    </item>
  </channel>
</rss>
