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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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360 topics in this forum

  1. Do Not Use Unauthorized Devices for Measuring Blood Pressure: FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 160 views

  3. Electrical Wheelchair Component Correction: mo-Vis BVBA Issues Correction for R-net Joysticks Due to a Firmware Error

    By FDA Recalls,
    • 0 replies
    • 185 views

  4. Early Alert: Medline Kits May Contain Recalled Medtronic Cardiac Cannulas

    By FDA Recalls,
    • 0 replies
    • 179 views

  5. Continuous Glucose Monitor Apps Correction: Dexcom, Inc. Issues Correction for G7 Apps and ONE+ Apps due to a Software Design Error That Does Not Alert Users of Unexpected Sensor Failure

    By FDA Recalls,
    • 0 replies
    • 180 views

  6. Insulin Pump Correction: Tandem Diabetes Care Issues Correction for Certain t:slim X2 Insulin Pumps Due to Risk for Faulty Speaker Wiring That May Cause Malfunction and Stop Insulin Delivery

    By FDA Recalls,
    • 0 replies
    • 151 views

  7. BD Provides Update on Voluntary Recall of Certain BD Alaris™ Pump Infusion Sets

    By FDA Recalls,
    • 0 replies
    • 178 views

  8. Insulin Pump Correction: Tandem Diabetes Care Issues Correction for Certain t:slim X2 Insulin Pumps Due to Risk for Faulty Speaker Wiring That May Cause Malfunction and Stop Insulin Delivery

    By FDA Recalls,
    • 0 replies
    • 150 views

  9. Ventilator Recall: Philips Respironics Removes Certain DreamStation Devices Due to Programming Errors That Can Result in Failed Therapy Modes

    By FDA Recalls,
    • 0 replies
    • 152 views

  10. Update on Alert: Defibrillation Lead Issue from Boston Scientific

    By FDA Recalls,
    • 0 replies
    • 181 views

  11. Update on Alert: Defibrillation Lead Issue from Boston Scientific

    By FDA Recalls,
    • 0 replies
    • 186 views

  12. Continuous Glucose Monitor Apps Correction: Dexcom, Inc. Issues Correction for G7 Apps and ONE+ Apps due to a Software Design Error That Does Not Alert Users of Unexpected Sensor Failure

    By FDA Recalls,
    • 0 replies
    • 179 views

  13. Ventilator Recall: Philips Respironics Removes Certain DreamStation Devices Due to Programming Errors That Can Result in Failed Therapy Modes

    By FDA Recalls,
    • 0 replies
    • 163 views

  14. Анализ посещения сайтов в Москве

    By Analiz_ussi,
    • 0 replies
    • 205 views

  15. Mobile Power Unit AC Power Cord Recall: Abbott Medical Removes AC Power Cord Associated with HeartMate Mobile Power Unit (MPU) Due to Potential Risk of the Cord Not Locking into Place

    By FDA Recalls,
    • 0 replies
    • 239 views

  16. Manual Resuscitator Recall: Ambu Inc. Removes SPUR II Resuscitators Due to Blocked Manometer Port

    By FDA Recalls,
    • 0 replies
    • 205 views

  17. Breathing Circuit Set Recall: Hamilton Medical, Inc. Removes Coaxial Breathing Circuit Set Due to Possible Inner Blue Tube Cracks That May Impact Ventilation

    By FDA Recalls,
    • 0 replies
    • 214 views

  18. Green Lumber Holding, LLC Issues Consumer Alert on Counterfeit Products Following FDA Findings

    By FDA Recalls,
    • 0 replies
    • 240 views

  19. Infusion Pump Correction: ICU Medical, Inc. Issues Correction for Plum Duo Infusion System Due to Software Possibly Resulting in Pump Becoming Unresponsive

    By FDA Recalls,
    • 0 replies
    • 164 views

  20. DermaRite Industries Expands Voluntary Nationwide Recall Due to Potential Burkholderia cepacia Contamination

    By FDA Recalls,
    • 0 replies
    • 176 views

  21. Ventilator Correction: Hamilton Medical AG Corrects HAMILTON-C6 Due to Risk of Ventilation Interruption from Defective Circuit Board

    By FDA Recalls,
    • 0 replies
    • 208 views

  22. Applicator Recall: Integra LifeSciences Removes Extended Tip Applicator Due to Potential Sterility and Endotoxin Concerns

    By FDA Recalls,
    • 0 replies
    • 172 views

  23. Unichem Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Cyclobenzaprine Hydrochloride Tablets USP 10 mg, Due to Mislabeling

    By FDA Recalls,
    • 0 replies
    • 175 views

  24. FDA Update on the Safety of Ixchiq (Chikungunya Vaccine, Live). FDA Suspends Biologics License: FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 306 views

  25. Follow Instructions for Safe Use of Hyperbaric Oxygen Therapy Devices - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 210 views

  26. Vascular Stent Recall: Boston Scientific Removes Carotid WALLSTENT Monorail Endoprosthesis Due to Risk of Resistance During Device Withdrawal

    By FDA Recalls,
    • 0 replies
    • 226 views
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