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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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436 topics in this forum

  1. Early Alert: Microbore Extension Set Issue from B. Braun Medical Inc.

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    • 284 views

  3. Endoscopic Vessel Harvesting (EVH) System Correction: Getinge and Maquet Cardiovascular Update Use Instructions for VasoView HemoPro 2 (VH-4000 and VH-4001) EVH Systems due to Risk for Bent or Detached Heater Wires and Silicone Peeling or Detaching During

    By FDA Recalls,
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    • 241 views

  4. Early Alert: Infusion Set Performance Issue from BD

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    • 260 views

  5. Nostrum Laboratories, Inc. Issues Voluntary Nationwide Recall of Sucralfate Tablets USP 1 Gram Within Expiry

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    • 301 views

  6. Closed Suction Catheter Recall: Avanos Medical, Inc. Removes Ballard Closed Suction Systems Due to Risk of Non-Sterility

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    • 291 views

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

    By FDA Recalls,
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    • 259 views

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

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    • 236 views

  9. Early Alert: Infusion Pump Software Issue from Baxter

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    • 265 views

  10. Early Alert: Blood Pump Controller Issue from Abiomed

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    • 355 views

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

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    • 304 views

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

    By FDA Recalls,
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    • 453 views

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

    By FDA Recalls,
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    • 269 views

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

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    • 256 views

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

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    • 345 views

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

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    • 294 views

  17. 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 

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    • 218 views

  18. 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,
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    • 333 views

  19. 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,
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    • 235 views

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

    By FDA Recalls,
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    • 295 views

  21. 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,
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    • 213 views

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

    By FDA Recalls,
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    • 250 views

  23. 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,
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    • 256 views

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

    By FDA Recalls,
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    • 252 views

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

    By FDA Recalls,
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    • 273 views

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

    By FDA Recalls,
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    • 277 views
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