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Recalls

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

109 topics in this forum

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

    By FDA Recalls,
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    • 46 views

  2. 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
    • 48 views

  3. 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,
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    • 36 views

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

    By FDA Recalls,
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    • 34 views

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

    By FDA Recalls,
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    • 60 views

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

    By FDA Recalls,
    • 0 replies
    • 50 views

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

    By FDA Recalls,
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    • 68 views

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

    By FDA Recalls,
    • 0 replies
    • 59 views

  9. 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
    • 57 views

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

    By FDA Recalls,
    • 0 replies
    • 77 views

  11. 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,
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    • 62 views

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

    By FDA Recalls,
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    • 86 views

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

    By FDA Recalls,
    • 0 replies
    • 89 views

  14. 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
    • 69 views

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

    By FDA Recalls,
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    • 64 views

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

    By FDA Recalls,
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    • 66 views

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

    By FDA Recalls,
    • 0 replies
    • 81 views

  18. 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
    • 64 views

  19. 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
    • 57 views

  20. Staska Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Ascorbic Acid Solution for Injection (Preservative Free, Non-Corn) 500mg/mL Due to the Presence of Glass Particles

    By FDA Recalls,
    • 0 replies
    • 61 views

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

    By FDA Recalls,
    • 0 replies
    • 50 views

  22. C&A Naturistics Issues Voluntary Nationwide Recall of AK Forte Tablets con Ortiga y Omega 3 Due to the Presence of Undeclared Drug Ingredients: Diclofenac, Dexamethasone, and Methocarbamol

    By FDA Recalls,
    • 0 replies
    • 59 views

  23. Infusion Pump Recall: Zyno Medical Removes Z-800, Z-800F, Z-800W, and Z800WF Infusion Pumps due to an Air-in-Line Software Defect That May Allow Larger than Expected Air Bubbles to Enter Patients

    By FDA Recalls,
    • 0 replies
    • 81 views

  24. Resuscitator Recall: Mercury Medical Removes Neo-Tee T-Piece Resuscitators due to Risk of Inline Controller Detachment that May Impact Ventilation

    By FDA Recalls,
    • 0 replies
    • 74 views

  25. Philips Respironics Issues Additional Usage Instructions for Trilogy Evo Ventilators Related to Use of In-Line Nebulizers

    By FDA Recalls,
    • 0 replies
    • 64 views
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