Medical Device Recalls
-
1 result found
PMA Number: P960040/S053 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VITALITY HE (model T180) Implantable Cardioverter Defibrillator (ICD). Sterile EO. Guidant Corporat... | 2 | 07/04/2006 | Guidant Corporation |
-