Two Class I Designations Assigned to DePuy Synthes Recalls of CMF Distraction System Jaw-Stabilizing Device
Deaths Involved DePuy Synthes CMF. Parker Waichman LLP is reviewing claims concerning serious injuries and deaths involving the DePuy Synthes Craniomaxillofacial (CMF) Distraction System Jaw-Stabilizing device. DePuy Synthes is a unit of healthcare giant Johnson & Johnson. The DePuy Synthes CMF Distraction System (AB … [Read more...] about Two Class I Designations Assigned to DePuy Synthes Recalls of CMF Distraction System Jaw-Stabilizing Device
DePuy Synthes Power Tool Battery Recall
Recalled Devices Cause Serious Injuries or Death - Findings. Medical device maker DePuy Synthes has recalled power sources for surgical power tool systems because these components could explode. The Food and Drug Administration (FDA) has identified this as a Depuy Synthes Class I recall, the most serious type of recall. Use of … [Read more...] about DePuy Synthes Power Tool Battery Recall
Most-Serious Class I Label on J&J’s DePuy Synthes Recall
J&J's DePuy Synthes Recall Gets Serious Attention. The U.S. Food and Drug Administration (FDA) has placed its most-serious Class I label on Johnson & Johnson’s DePuy Synthes recall of its jaw-stabilizing device. A Class I designation is the FDA’s most serious recall status; it means that use of the recalled device has … [Read more...] about Most-Serious Class I Label on J&J’s DePuy Synthes Recall
DePuy Synthes Recall is Labeled as Class I, Risk of Airway Obstruction
FDA considers this most serious recall status. DePuy’s recall of the Synthes Craniomaxillofacial (CMF) Distraction System (AB Distractor Bodies and BC Distractor Bodies) has been deemed Class I by the U.S. Food and Drug Administration (FDA); this is the most serious recall status, and indicates that the recalled device can cause … [Read more...] about DePuy Synthes Recall is Labeled as Class I, Risk of Airway Obstruction
