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Recalls

A list of FDA Recalls that is updated daily. It references medical equipment and medical product notifications and recalls.

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  1. Do Not Use Cue Health’s COVID-19 Tests Due to Risk of False Results: FDA Safety Communication

    By FDA Recalls,
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    • 568 views

  3. 2024 Safety Communications

    By FDA Recalls,
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    • 545 views

  4. Philips Respironics, Inc. Recalls Trilogy Evo Continuous Ventilators due to a Software-Related Possible Power Malfunction

    By FDA Recalls,
    • 0 replies
    • 793 views

  5. MEGADYNE™ Initiates Global Discontinuation and Voluntary Recall of MEGA SOFT™ Pediatric Patient Return Electrode

    By FDA Recalls,
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    • 692 views

  6. Route 92 Medical Inc. Recalls Catheter due to Distal Tip Separation at the Proximal Marker Band

    By FDA Recalls,
    • 0 replies
    • 702 views

  7. Tandem Diabetes Care, Inc. Recalls Version 2.7 of the Apple iOS t:connect Mobile App Used in Conjunction with t:slim X2 Insulin Pump with Control-IQ Technology Prompted by a Software Problem Leading to Pump Battery Depletion

    By FDA Recalls,
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    • 677 views

  8. 2024 Letters to Health Care Providers

    By FDA Recalls,
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    • 667 views

  9. Getinge/Maquet Cardiohelp System: Potential Insufficient Packaging Sterility with HLS Set Advanced - Letter to Health Care Providers

    By FDA Recalls,
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    • 656 views

  10. UPDATE: Risk of Device Failures for Getinge’s Maquet/Datascope Cardiosave Intra-Aortic Balloon Pump (IABP) – Letter to Health Care Providers

    By FDA Recalls,
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    • 757 views

  11. Oxygenator Devices Used for Extracorporeal Circulation - Letter to Health Care Providers

    By FDA Recalls,
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    • 577 views

  12. Safety and Quality Concerns with Getinge Cardiovascular Devices - Letter to Health Care Providers

    By FDA Recalls,
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    • 643 views

  13. BioMérieux Inc. Recalls VITEK 2 AST Kit due to Incorrect Ceftriaxone Concentrations

    By FDA Recalls,
    • 0 replies
    • 662 views

  14. SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty

    By FDA Recalls,
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    • 620 views

  15. SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a Partial Obstruction in 2.5mm Sensors and Up To 3mm Distal to the Sensor Tip

    By FDA Recalls,
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    • 640 views

  16. FDA Encourages the Public to Follow Established Choking Rescue Protocols: FDA Safety Communication

    By FDA Recalls,
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    • 511 views

  17. Elekta Instrument AB Recalls Disposable Biopsy Needle Kit for Leksell Stereotactic System for Possibly Containing Microscopic Stainless Steel Debris on the Inside of the Biopsy Needle

    By FDA Recalls,
    • 0 replies
    • 611 views

  18. Draeger, Inc. Recalls Perseus A500 Anesthesia System for Risk of Sudden Unexpected Shutdown When Used on Battery Power

    By FDA Recalls,
    • 0 replies
    • 551 views

  19. Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and Stay-Safe/Luer Lock Adapter for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA

    By FDA Recalls,
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    • 689 views

  20. UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication

    By FDA Recalls,
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    • 517 views

  21. Update: Potential Risk of Exposure to Toxic Compounds When Using Hemodialysis and Peritoneal Dialysis Systems – Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 715 views

  22. InfuTronix, LLC Recalls Nimbus and Nimbus II Infusion Pump Systems for Multiple Device Failures That May Cause Severe Injury and Death

    By FDA Recalls,
    • 0 replies
    • 456 views

  23. Outset Medical, Inc. Recalls Certain Tablo Hemodialysis Systems for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBAs

    By FDA Recalls,
    • 0 replies
    • 620 views

  24. DeRoyal Industries, Inc. Recalls Tracecarts Containing 16FR Urine Meter Foley Under Recall by Nurse Assist

    By FDA Recalls,
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    • 592 views

  25. STOP CLOPEZ CORP Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of Undeclared Nortadalafil

    By FDA Recalls,
    • 0 replies
    • 554 views

  26. Dr. Reddy’s Issues Voluntary Nationwide Recall of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg Due to Sub-Potency

    By FDA Recalls,
    • 0 replies
    • 678 views
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