The U.S. Food and Drug Administration (FDA) has issued a Class I recall for over 380,000 saline flush syringes after discovering the syringes were possibly contaminated with a dangerous...
The U.S. Food and Drug Administration (FDA) has identified a recall by DePuy Orthopedics as Class I, the most serious type of recall. The company is warning consumers the...
The FDA issued a Class I recall for the VentStar Oxylog 3000 Disposable Pediatric Patient Circuit manufactured by Dräger. More than 1,500 units are being recalled from hospitals in...
The U.S. Food and Drug Administration (FDA) recently announced the recall of the CareFusion AVEA Ventilator from the market. The AVEA ventilator is used in hospitals and healthcare centers...
