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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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  1. Broselow Pediatric Emergency Rainbow Tape Recall: AirLife Removes Certain Broselow Pediatric Emergency Rainbow Tapes due to Misprinted Information

    By FDA Recalls,
    • 0 replies
    • 310 views

  3. Infant Breathing System Recall: AirLife/Vyaire Removes Infant Heated Wire Circuits Due to Risk for Inadvertent Adapter Disconnection During Ventilation

    By FDA Recalls,
    • 0 replies
    • 285 views

  4. Early Alert: Infusion Pump Software Issue from Baxter

    By FDA Recalls,
    • 0 replies
    • 305 views

  5. Early Alert: Blood Pump Controller Issue from Abiomed

    By FDA Recalls,
    • 0 replies
    • 402 views

  6. Extended-Release Stimulants for ADHD: FDA Drug Safety Communication - FDA Requires Expanded Labeling about Weight Loss Risk in Patients Younger than 6 Years

    By FDA Recalls,
    • 0 replies
    • 353 views

  7. Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Cefazolin for Injection Due to Product Mispackaging

    By FDA Recalls,
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    • 497 views

  8. Angiographic Catheter Recall: Cook Removes Beacon Tip Angiographic Catheters due to Tip Separation

    By FDA Recalls,
    • 0 replies
    • 320 views

  9. mRNA COVID-19 Vaccines: FDA Safety Communication - FDA Approves Required Updated Warning in Labeling Regarding Myocarditis and Pericarditis Following Vaccination

    By FDA Recalls,
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    • 297 views

  10. Early Alert: Esophageal pH Monitoring Capsule Issue from Medtronic

    By FDA Recalls,
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    • 384 views

  11. Import Alerts for Certain Olympus Medical Devices Manufactured in Japan - Letter to Health Care Providers

    By FDA Recalls,
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    • 335 views

  12. Anesthesia Delivery Systems Recall: GE HealthCare Issues Correction for Certain Carestations due to Risk of Ineffective Ventilation When Used in Volume Control Ventilation (VCV) Mode 

    By FDA Recalls,
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    • 257 views

  13. Resuscitation System Recall: ZOLL Circulation, Inc. Recalls AutoPulse NXT Resuscitation System Due to a Failure Code That May Stop Compressions or Deliver Inadequate CPR

    By FDA Recalls,
    • 0 replies
    • 375 views

  14. Medical Procedure Kits Correction: Medline Industries, LP Issues Correction for Medline Procedure Kits Containing Medtronic Aortic Root Cannula due to Potential Excess Material in Male Luers

    By FDA Recalls,
    • 0 replies
    • 273 views

  15. Transderm Scōp (Scopolamine Transdermal System): Drug Safety Communication - FDA Adds Warning About Serious Risk of Heat-Related Complications with Antinausea Patch

    By FDA Recalls,
    • 0 replies
    • 340 views

  16. Convenience Kit Recall: Medline Industries, LP, Removes Medline Neonatal and Pediatric Kits containing Smiths Medical ORAL/NASAL Endotracheal Tubes Due to Smaller Than Expected Tube Diameter That May Cause Underventilation

    By FDA Recalls,
    • 0 replies
    • 261 views

  17. Blood Products Administration Set Recall: Fresenius Kabi Removes Large Volume Pump Blood Products Administration Sets due to Incorrect Assembly

    By FDA Recalls,
    • 0 replies
    • 287 views

  18. Aspiration Catheter Recall: Q’Apel Medical, Inc. Removes Hippo 072 Aspiration System and Cheetah Delivery Tool After FDA Warning Letter About Internal Processes and Distal Tip Characteristics

    By FDA Recalls,
    • 0 replies
    • 294 views

  19. Infusion Pump Recall: Zyno Medical Removes Certain Z-800 Series Infusion Pumps due to Software Issue

    By FDA Recalls,
    • 0 replies
    • 295 views

  20. Intra-Operative Positioning System Guidewire Recall: Centerline Biomedical Removes Certain IOPS Guidewires due to Delamination

    By FDA Recalls,
    • 0 replies
    • 307 views

  21. Liquid Bicarbonate Concentrate Recall: Nipro Removes MedicaLyte Liquid Bicarbonate Concentrate due to Contamination

    By FDA Recalls,
    • 0 replies
    • 309 views

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

    By FDA Recalls,
    • 0 replies
    • 333 views

  23. 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
    • 346 views

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

    By FDA Recalls,
    • 0 replies
    • 408 views

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

    By FDA Recalls,
    • 0 replies
    • 329 views
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