Jump to content
BMET Galaxy

Recalls

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

Guests need to register to view. 

458 topics in this forum

  1. 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
    • 267 views

  3. 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
    • 250 views

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

    By FDA Recalls,
    • 0 replies
    • 280 views

  5. 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
    • 260 views

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

    By FDA Recalls,
    • 0 replies
    • 224 views

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

    By FDA Recalls,
    • 0 replies
    • 280 views

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

    By FDA Recalls,
    • 0 replies
    • 244 views

  9. 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
    • 242 views

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

    By FDA Recalls,
    • 0 replies
    • 217 views

  11. Анализ посещения сайтов в Москве

    By Analiz_ussi,
    • 0 replies
    • 245 views

  12. 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
    • 310 views

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

    By FDA Recalls,
    • 0 replies
    • 283 views

  14. 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
    • 299 views

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

    By FDA Recalls,
    • 0 replies
    • 311 views

  16. 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
    • 234 views

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

    By FDA Recalls,
    • 0 replies
    • 253 views

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

    By FDA Recalls,
    • 0 replies
    • 290 views

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

    By FDA Recalls,
    • 0 replies
    • 258 views

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

    By FDA Recalls,
    • 0 replies
    • 254 views

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

    By FDA Recalls,
    • 0 replies
    • 398 views

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

    By FDA Recalls,
    • 0 replies
    • 291 views

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

    By FDA Recalls,
    • 0 replies
    • 299 views

  24. B. Braun Medical Issues Voluntary Nationwide Recall of Lactated Ringer’s Injection USP 1000 mL and 0.9% Sodium Chloride Injection USP 1000 mL Due to the Presence of Particulate Matter

    By FDA Recalls,
    • 0 replies
    • 302 views

  25. Early Alert: Infusion Pump Issue from Baxter

    By FDA Recalls,
    • 0 replies
    • 276 views

  26. Early Alert: Cardiac Cannula Issue from Medtronic

    By FDA Recalls,
    • 0 replies
    • 258 views
×
×
  • Create New...