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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. Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

    By FDA Recalls,
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    • 232 views

  3. Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination

    By FDA Recalls,
    • 0 replies
    • 254 views

  4. Infusion Pump Correction: Baxter Updates Instructions for Use for Novum IQ Large Volume Pump due to Potential for Underinfusion

    By FDA Recalls,
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    • 325 views

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  6. Infusion Pump Recall: Infusion Pump Thermal Damage Issue from Smiths Medical

    By FDA Recalls,
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    • 233 views

  7. Anesthesia Breathing Circuit Kit Correction: Draeger, Inc. Updates Use Instructions for VentStar Flex and Anesthesia Circuit Kits Due to Cracks in Hose That May Cause Inadequate Ventilation

    By FDA Recalls,
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    • 233 views

  8. Infusion Pump Recall: False Alarm Issue with Infusion Pump from Smiths Medical

    By FDA Recalls,
    • 0 replies
    • 241 views

  9. Infusion Pump Recall: Infusion Pump Intermittent Connection Issue from Smiths Medical

    By FDA Recalls,
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    • 224 views

  10. Flexible Tracheostomy Tube Recall: Medtronic Removes Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula Due to Risk for Disconnection of the Flange from the Device Cannula

    By FDA Recalls,
    • 0 replies
    • 239 views

  11. Amneal Pharmaceutical LLC Issues a Nationwide Recall of Sulfamethoxazole / Trimethoprim Tablets, USP, 400 mg/80 mg Only, Due to Microbial Contamination

    By FDA Recalls,
    • 0 replies
    • 225 views

  12. Risk of False Positive Lead Test Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 243 views

  13. Cetirizine or Levocetirizine: Drug Safety Communication - FDA Warns About Risk of Severe Itching After Discontinuation of Long-Term Use of Allergy Medicines

    By FDA Recalls,
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    • 319 views

  14. Esophagogastric Tube Recall: BD Issues Correction for Esophagogastric Balloon Tamponade Tubes due to Challenges Removing Plastic Plugs from Rubber Lumen

    By FDA Recalls,
    • 0 replies
    • 228 views

  15. UMARY- USA.COM Issues Voluntary Nationwide Recall of UNAVY ÁCIDO HIALURÓNICO Caplets and UMOVY ÁCIDO HIALURÓNICO Caplets Due to the Presence of Undeclared Drug Ingredients Dexamethasone, Diclofenac and Omeprazole

    By FDA Recalls,
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    • 182 views

  16. FDA and CDC Recommend Pause in Use of Ixchiq (Chikungunya Vaccine, Live) in Individuals 60 Years of Age and Older While Postmarketing Safety Reports are Investigated: FDA Safety Communication

    By FDA Recalls,
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    • 216 views

  17. FDA Advises Consumers, Tattoo Artists, and Retailers to Avoid Using or Selling Certain Sacred Tattoo Ink Products Contaminated with Microorganisms

    By FDA Recalls,
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    • 297 views

  18. EnShiShiXiangNiShangMaoYouXianGongSi Issues Voluntary Nationwide Recall of ENDURANCE BOOST WITH HORNY GOAT WEED Capsules Due To Presence of Undeclared Propoxyphenylsildenafil and Sildenafil

    By FDA Recalls,
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    • 231 views

  19. Heart Pump Accessory Removal: Abbott Removes HeartMate Mobile Power Unit due to Instances of Sudden Power Loss

    By FDA Recalls,
    • 0 replies
    • 233 views

  20. Risk of False Positive Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication

    By FDA Recalls,
    • 0 replies
    • 260 views

  21. Early Alert: Intravascular PICC Catheter Issue from BD

    By FDA Recalls,
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    • 242 views

  22. Early Alert: Diagnostic Intravascular Catheter Issue from Conavi

    By FDA Recalls,
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    • 245 views

  23. FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I

    By FDA Recalls,
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    • 283 views

  24. Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter

    By FDA Recalls,
    • 0 replies
    • 251 views

  25. Bausch + Lomb Announces Voluntary Recall of enVista Aspire™, enVista Envy™ and Certain enVista® Monofocal Intraocular Lenses in the U.S.

    By FDA Recalls,
    • 0 replies
    • 312 views

  26. Max Mobility / Permobil Expands Nationwide Recall of SmartDrive Speed Control Dial Due to the Motor Being Unresponsive to the User

    By FDA Recalls,
    • 0 replies
    • 351 views
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