Teleflex announced the worldwide voluntary recall of Hudson RCI Pediatric Anesthesia Breathing Circuits, which the U.S. Food and Drug Administration has classified as a Class 1 recall. The FDA defines ...

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated announced today that the U.S. Food and Drug Administration (FDA) has classified the voluntary medical device recall of Hudson RCI® Pediatric ...

Draeger Medical, or Dräger US, recalled more than half a million airway devices because of a manufacturing error that can lead to hypoxia and death, the FDA said May ...

Child-anesthesia-technology-enhances-surgical-accuracy-early-complication-detection-and-pain-assessment-for-safer-recovery ...