The U.S. Food and Drug Administration (FDA) reported on its website that St. Jude Medical Inc. recalled the wire that is used to place a device which closes the openings between the two upper...
DePuy Recalls Knee Device for Potential of Fracture
The U.S. Food and Drug Administration (FDA) has notified healthcare providers that DePuy Orthopaedics has issued a Class I recall of its LPS Disphyseal Sleeve orthopedic knee device due to a...
Scuba Diving Tubing Recalled Because of Drowning Hazard
Some products we use are meant to keep us safe even during new and dangerous adventures such as deep sea diving. Unfortunately, though, some products may contain defects that make them unsafe and can prevent a dangerous hazard.
Scuba Diving Hose...