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Purge cassette recognition failures involving Automated Impella Controllers may delay or interrupt critical mechanical circulatory support for seriously ill cardiac patients. What …

Patients May Face Dangerous Oxygen Deprivation When Recalled Hamilton Medical Coaxial Breathing Circuit Sets Obstruct Exhalation – Serious Brain Injuries Reported. What …

Nearly 11,000 Philips Interventional Systems Reportedly Affected by Software Problems That Can Degrade Images or Stop Equipment Movement During Patient Procedures. What …

Omnipod 5 Insulin Pump Pods Recalled Following Reports of Serious Injuries What Parker Waichman LLP Found The FDA designated the Omnipod 5 …

ResMed Astral 100 and Astral 150 Ventilator Correction May Leave Patients Vulnerable to Life-Threatening Therapy Interruptions What Parker Waichman LLP Found Certain …

FDA Warning Issued for Boston Scientific Enroute Transcarotid Neuroprotection Systems Following Serious Device Failure What Parker Waichman LLP Found The FDA instructed …

Boston Scientific ENROUTE Transcarotid Neuroprotection System Recall May Put Patients at Risk of Stroke and Other Serious Complications. What Parker Waichman LLP …

FDA Class I Recall Issued After Contaminated Bupivacaine in Certain B. Braun Convenience Kits Is Linked to Serious Injuries and Potential Life-Threatening …

Healthcare Providers Are Now Being Urged to Return Unused Devices Immediately Following Updated FDA Safety Guidance Involving Life-Threatening Device Malfunctions What Parker …

FDA Issues Most Serious Recall Classification After Software Error in Automated Impella Controllers Linked to Reported Injuries and Death What Parker Waichman …