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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. Vascular Cannula Recall: Medtronic Removes Aortic Root Cannula Due to Unexpected Loose Material in the Male Luer

    By FDA Recalls,
    • 0 replies
    • 280 views

  3. Safe Use of Megadyne Mega 2000 and Mega Soft Patient Return Electrodes - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 243 views

  4. Endotracheal Tube Recall: Smiths Medical Removes Intubation ORAL/NASAL Endotracheal Tubes Due to Smaller Than Expected Tube Diameter That May Cause Underventilation

    By FDA Recalls,
    • 0 replies
    • 301 views

  5. Update on Alert: Atherectomy Catheter System Issue from Bard Peripheral Vascular

    By FDA Recalls,
    • 0 replies
    • 286 views

  6. Infusion Pump Software Correction: Becton, Dickinson and Company (BD) Issues Correction for BD Alaris Systems Manager and Care Coordination Engine Infusion Adapter Software Due to Risk for Outdated Automated Programming Requests to Load

    By FDA Recalls,
    • 0 replies
    • 724 views

  7. Early Alert: Aspiration System Issue from Calyxo

    By FDA Recalls,
    • 0 replies
    • 330 views

  8. Update on Alert: Infusion Pump Issue from Baxter Healthcare Corporation

    By FDA Recalls,
    • 0 replies
    • 263 views

  9. Implantable Port Recall: Smiths Medical Removes ProPort Plastic Implantable Ports Due to Manufacturing Error that May Cause Separation

    By FDA Recalls,
    • 0 replies
    • 311 views

  10. Embolization Device Recall and Correction: Medtronic Removes Unused 027 Compatible Pipeline Vantage Embolization Device with Shield Technology, Updates Use Instructions for 021 Compatible Pipeline Vantage Embolization Devices due to Increased Risk of Inco

    By FDA Recalls,
    • 0 replies
    • 246 views

  11. Disruptions in Availability of Hemodialysis Bloodlines - Letter to Health Care Providers

    By FDA Recalls,
    • 0 replies
    • 319 views

  12. Dr. Reddy’s Issues a Nationwide Recall of Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL, in the U.S., Due to Mislabeling of Infusion Bag

    By FDA Recalls,
    • 0 replies
    • 248 views

  13. Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC): Voluntary Lot Withdrawals - Due to Increased Reports of Allergic/Hypersensitivity Reactions

    By FDA Recalls,
    • 0 replies
    • 252 views

  14. Smiths Medical Issues Urgent Medical Device Correction Informing Customers of a Potential Issue with Certain Sizes of Intubation ORAL/NASAL Endotracheal Tubes Being Smaller Than Expected

    By FDA Recalls,
    • 0 replies
    • 331 views

  15. Early Alert: Infusion Pump Issue from Baxter Healthcare Corporation

    By FDA Recalls,
    • 0 replies
    • 334 views

  16. Update on Alert: Solution Set Issue from Baxter Healthcare Corporation

    By FDA Recalls,
    • 0 replies
    • 289 views

  17. Update on Alert: Infusion Pump Software Issue from Fresenius Kabi USA

    By FDA Recalls,
    • 0 replies
    • 311 views

  18. Endovascular System Recall: Philips Removes and Discontinues Distribution of Tack Endovascular System Due to User Challenges That Caused Additional Procedures to Reposition or Remove Implant

    By FDA Recalls,
    • 0 replies
    • 272 views

  19. One Source Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

    By FDA Recalls,
    • 0 replies
    • 297 views

  20. Vaporizer Recall: Getinge Removes Vaporizer Sevoflurane Quick-Fil and Expands Recall of Vaporizer Sevoflurane Maquet Filling due to Risk of Patient and Health Care Professional Exposure to Toxic Chemical Hydrogen Fluoride

    By FDA Recalls,
    • 0 replies
    • 238 views

  21. Power Assist Device Recall: Max Mobility/Permobil Removes SpeedControl Dial Component Used with SmartDrive MX2+ Power Assist Device Due to Risk for Motor to Be Unresponsive to the User

    By FDA Recalls,
    • 0 replies
    • 247 views

  22. Patient Table Correction: Philips Updates Use Instructions for Allura and Azurion Systems due to Patient Fall Risk from Incorrectly Positioned Mattresses

    By FDA Recalls,
    • 0 replies
    • 305 views

  23. Ablation Catheter Correction: Biosense Webster Updates Use Instructions for Varipulse due to High Rate of Stroke or Transient Ischemic Attack

    By FDA Recalls,
    • 0 replies
    • 364 views

  24. Endoscope Instrument Recall: Olympus Removes Single Use Guide Sheath Kits Due to Risk for Radiopaque Guide Sheath Tip Detaching During Procedures

    By FDA Recalls,
    • 0 replies
    • 270 views

  25. Regard Newborn Kit Recall: ROi CPS, LLC Removes Certain Newborn Kits Due to a Recalled Component, the Neo-Tee T-Piece Resuscitator With An Undersized Controller Spring

    By FDA Recalls,
    • 0 replies
    • 280 views

  26. Natural Dior LLC Issues Voluntary Nationwide Recall of Vitafer-L Gold Liquid Due to Presence of Undeclared Tadalafil

    By FDA Recalls,
    • 0 replies
    • 291 views
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