Medical Device Recalls
-
11 to 12 of 12 Results
Recall Date to: 07%2F14%2F2014 PMA Number: P060040 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
HeartMate II System Controller Product Usage: HeartMate II is a mechanical device that circulate... | 1 | 03/21/2014 | Thoratec Corporation |
HeartMate II Left Ventricular Assist System (HM II LVAS) Sealed Outflow Graft Bend Relief. The Seal... | 1 | 03/23/2012 | Thoratec Corporation |
-