Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K870562 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Enpath Lead Adapter, Ref: 501214. The contents of the inner package have been sterilized by ethylen... | 2 | 12/29/2009 | Greatbatch Medical |
Enpath Lead Adapters, pacemaker lead adapter. Affects: 5 mm Bipolar, Model 501205; 6 mm Unipolar,... | 2 | 11/09/2006 | Enpath Medical, Inc |
-