Tag:
Class I recall
Latest Headlines
Latest Headlines
FDA classifies St. Jude's Riata lead recall as Class I
The FDA has classified St. Jude Medical's ( $STJ ) voluntary medical device advisory letter to physicians from Nov. 28 relating to its Riata and Riata ST silicone defibrillation leads as a Class I
Boston Sci recalls imaging catheters
Boston Scientific announced Friday that it is voluntarily recalling more than 29,000 iCross coronary imaging catheters distributed in the U.S., Puerto Rico, Trinidad, Tobago and the American Virgin
Davol's XenMatrix recalled on toxin concerns
The FDA has issued a Class I recall notice of a cloth-like surgical device made by C.R. Bard subsidiary Davol. XenMatrix Surgical Graft is used to treat hernia and abdominal wall repair, notes
Arstasis arterial access device recalled for faulty parts
The FDA has issued a Class I recall for Arstasis's One Access System recall device after reports that device components may separate during procedures. The device is used during femoral artery
FDA classifies Medtronic tissue stabilizer recall as Class I
The FDA has classified the Medtronic's previous action related to the Octopus Nuvo tissue stabilizer, which is used to stabilize tissue during certain surgical procedures, as a Class I recall. The
