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Medtronic Recalls More Than 50,000 Arterial Cannulae After Reports of Leaks During Cardiopulmonary Bypass Procedures FDA Class II Recall Raises Concerns About …

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

Federal Health Officials Warn That Inflatable Baby Neck Floats May Pose Drowning, Suffocation, and Neck Injury Risks While Marketing Claims Remain Unproven …

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

FDA Class II Recall Raises Questions About Product Safety, Potential Eye Infections, and the Legal Rights of Consumers Who Suffered Injuries What …

Dabigatran (Generic Pradaxa) Recalled After Cases of Blood Clots And What Parker Waichman LLP Found The FDA recalled specific lots of generic …

FDA Safety Alert Raises New Concerns About Tavneos After Reports of Fatal Liver Injuries What Parker Waichman LLP Found The FDA identified …

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

How the CPSC’s New NEISS-R Injury Surveillance System Could Improve Product Safety and Help Prevent Serious Injuries Nationwide What Parker Waichman LLP …

Eight toddler tower models have been recalled following more than 100 reported safety incidents, including falls, collapses, tip-overs, entrapments, and injuries to …