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. 

390 topics in this forum

  1. Early Alert: TactiFlex Ablation Catheter Issue from Abbott

    By FDA Recalls,
    • 0 replies
    • 188 views

  3. FDA Updates Warning About Imported Cookware That May Leach Lead: August 2025

    By FDA Recalls,
    • 0 replies
    • 181 views

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

    By FDA Recalls,
    • 0 replies
    • 186 views

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

    By FDA Recalls,
    • 0 replies
    • 191 views

  6. Do Not Use Unauthorized Infant Devices for Monitoring Vital Signs: FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 187 views

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

    By FDA Recalls,
    • 0 replies
    • 180 views

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

    By FDA Recalls,
    • 0 replies
    • 199 views

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

    By FDA Recalls,
    • 0 replies
    • 195 views

  10. 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
    • 208 views

  11. 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
    • 169 views

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

    By FDA Recalls,
    • 0 replies
    • 210 views

  13. 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
    • 173 views

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

    By FDA Recalls,
    • 0 replies
    • 174 views

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

    By FDA Recalls,
    • 0 replies
    • 212 views

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

    By FDA Recalls,
    • 0 replies
    • 203 views

  17. 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
    • 201 views

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

    By FDA Recalls,
    • 0 replies
    • 183 views

  19. Анализ посещения сайтов в Москве

    By Analiz_ussi,
    • 0 replies
    • 222 views

  20. 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
    • 262 views

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

    By FDA Recalls,
    • 0 replies
    • 231 views

  22. 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
    • 238 views

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

    By FDA Recalls,
    • 0 replies
    • 268 views

  24. 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
    • 188 views

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

    By FDA Recalls,
    • 0 replies
    • 204 views

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

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