Class I Recall - Due to Risk of Leaks That May Expose Providers and Patients to Hazardous/Toxic Substances
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Class I Recall - Due to Risk of Incorrect Intracranial Pressure Readings
Class I Recall - Due to Potential Water Ingress that May Cause Breathing Support to Stop
Class I Recall - Due to Faster Than Expected Flow Rates That May Impact Infusion Delivery
Class I Recall - Due to Electrical Faults That Cause Battery Failure
Recall - Due To The Potential Presence of Visible Particulates
Class I Recall - Due to Risk that Devices May Issue a Short Circuit Alert and Deliver Reduced Energy Shock During High Voltage Therapy
Class I Recall - Due to Catheter Hub Defect
Recall Expansion - Due to Potential for Microbial Contamination
Class I Recall - Due to Issues That May Cause Delayed Treatment Delivery
Class I Recall - Because They Are Not Authorized, Cleared, or Approved by the FDA
Recall - Due to the Presence of Undeclared Tadalafil in United States and Canada
Recall - Due to Microbial Contamination
Recall - Due To The Potential For Microbial Contamination
Recall - Due to Presence of Undeclared Sildenafil
Class I Recall - Tests Kits that Are Not Authorized, Cleared, or Approved by the FDA
Recall - Due to the Presence of Benzene
Recall - Due to the Presence of Undeclared Tadalafil
Recall Expansion - Due to Microbial Contamination
Class I Recall - Due to Risk of Medication Label Errors
Recall - Due to Products Stored Outside of Temperature Requirements
Class I Recall - Due to Software Issues That May Impact Infusion Delivery
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