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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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390 topics in this forum

  1. Syringe Recall: Cardinal Health Removes Certain Monoject U-100 mL Insulin Syringe Luer Lock with Tip Cap Soft Packs due to Incompatibility with Needleless Connectors

    By FDA Recalls,
    • 0 replies
    • 400 views

  3. Biopsy Needle Recall: Elekta Removes Disposable Biopsy Needle Kits due to Risk of Microscopic Stainless Steel Debris Inside Needle

    By FDA Recalls,
    • 0 replies
    • 423 views

  4. Hemodialysis Correction: Baxter Issues Correction for AK 98 Hemodialysis Machines Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs

    By FDA Recalls,
    • 0 replies
    • 398 views

  5. Insertion Tube Recall: FHC Removes microTargeting Insertion Tube Sets due to a Manufacturing Size Error That May Lead to Patient Harm

    By FDA Recalls,
    • 0 replies
    • 401 views

  6. Peritoneal Dialysis Set Correction: Baxter Issues Correction for MiniCap Extended Life Peritoneal Dialysis Transfer Sets Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs

    By FDA Recalls,
    • 0 replies
    • 432 views

  7. Mxbbb Issues Voluntary Nationwide Recall of Umary Acid Hyaluronic Due to the Presence of Diclofenac and Omeprazole

    By FDA Recalls,
    • 0 replies
    • 428 views

  8. Endo Expands Voluntary Recall of Clonazepam Orally Disintegrating Tablets, USP (C-IV) Due to Potential Product Carton Strength Mislabeling

    By FDA Recalls,
    • 0 replies
    • 401 views

  9. Anesthesia Machine Correction: Draeger, Inc., Issues Correction for Atlan A350 and A350 XL Anesthesia Workstations Due to Possible Mechanical Ventilation Failure

    By FDA Recalls,
    • 0 replies
    • 401 views

  10. Battery Pack Correction: Smiths Medical Updates Use Instructions for CADD-Solis Li-ion Rechargeable Battery Packs Due to Risk That Pack Damage May Cause a Circuit Short and Prevent Recharge

    By FDA Recalls,
    • 0 replies
    • 416 views

  11. Ventilator Correction: Philips Updates Use Instructions for Trilogy Evo, EvoO2, EV300, Evo Universal, Aeris EVO, Garbin Evo, and LifeVent EVO2 due to Risk of Inaccurate Flow Measurements Caused By Certain In-Line Nebulizer Placements

    By FDA Recalls,
    • 0 replies
    • 486 views

  12. Safety and Availability Concerns with VasoView HemoPro Endoscopic Vessel Harvesting Systems - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 451 views

  13. Endoscopic Vessel Harvesting System Recall: Getinge and Maquet Cardiovascular Remove VasoView HemoPro 1 and 1.5 Endoscopic Vessel

    By FDA Recalls,
    • 0 replies
    • 461 views

  14. Evaluation of Airborne Chemicals from Neonatal Incubators - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 440 views

  15. VitalityVita Issues Voluntary Nationwide Recall of VitalityXtra and PeakMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac

    By FDA Recalls,
    • 0 replies
    • 479 views

  16. Boulla LLC Issues Voluntary Nationwide Recall of ZoomMax and ZapMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac

    By FDA Recalls,
    • 0 replies
    • 470 views

  17. IPV Therapy Device Recall: Percussionaire Removes Certain Phasitron 5 Breathing Circuits Due to Risk of Nickel Exposure

    By FDA Recalls,
    • 0 replies
    • 392 views

  18. Incubator/Warmer Correction: GE Healthcare Updates Use Instructions for Giraffe OmniBed and Giraffe Omnibed CareStation due to Risk of Heater Door Falling and Causing Infant Injury

    By FDA Recalls,
    • 0 replies
    • 461 views

  19. Update: Use of GE HealthCare EVair and EVair 03 Compressors - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 454 views

  20. Air Compressor Device Correction: GE HealthCare Provides Updates to EVair Compressors Due to Final Formaldehyde Testing Results

    By FDA Recalls,
    • 0 replies
    • 428 views

  21. Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 476 views

  22. Assistive Arm Correction: Kinova Issues Correction for Jaco Assistive Robotic Arm due to Fire Hazard and Burn Risk

    By FDA Recalls,
    • 0 replies
    • 501 views

  23. Tracheostomy Tube Recall: Smiths Medical Removes BLUselect, BLUgriggs, and BLUperc Tracheostomy Tube Kits due to Potential Disconnection of Pilot Balloon

    By FDA Recalls,
    • 0 replies
    • 414 views

  24. Vascular Embolization Device Correction: Boston Scientific Updates Use Instructions for Obsidio Conformable Embolic for Increased Ischemia Risk When Used for GI Bleeding

    By FDA Recalls,
    • 0 replies
    • 374 views

  25. Voluntary Recall Notifying Medtronic Insulin Pump Users of Potential Risks of Shortened Pump Battery Life

    By FDA Recalls,
    • 0 replies
    • 461 views

  26. Insulin Pump Recall: Medtronic Notifies Users of MiniMed 600 and 700 Series Pumps of Risk of Shorter than Expected Battery Life

    By FDA Recalls,
    • 0 replies
    • 437 views
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