Medtronic Initiates Voluntary Field Actions for Selected Heparin-Coated Products Used During Cardiopulmonary Bypass
No commentsFOR IMMEDIATE RELEASE — MINNEAPOLIS – May 7, 2008 – Medtronic, Inc. today announced that it is initiating a voluntary and precautionary recall of selected products featuring the Carmeda BioActive surface. The affected devices are disposable products used [...]
FDA MedWatch- LifePak CR Plus Automated External Defibrillators- Class I Recall Because The Shock Button Is Not
1 comment so farFDA MedWatch- LifePak CR Plus Automated External Defibrillators- Class I Recall Because The Shock Button Is Not Visible Which Impedes Responder’s Ability To Provide Shock Therapy body { font-size: 12px; font-family: arial, verdana, sans-serif; font-weight: normal; font-style: normal; } .physicalAddress { color: gray; font-size: 10px; font-family: arial, verdana, sans-serif; font-weight: 100; }
Physio [...]
Baxter to Proceed with Recall of Remaining Heparin Sodium Vial Products
No commentsFOR IMMEDIATE RELEASE — DEERFIELD, Ill., February 28, 2008 – Baxter International Inc. announced today that the company is proceeding with the voluntary recall of all remaining lots and doses of its heparin sodium injection multi-dose, single-dose vials and HEP-LOCK heparin flush products. The company initially recalled nine lots of heparin sodium injection multi-dose [...]