Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K850505 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BD Perisafe catheter with catheter connector. The catheter connector has four components: body (gr... | 2 | 02/04/2006 | Becton Dickinson & Company |
BD Perisafe epidural mini-kit: 18 G x 3 1/2 in. Weiss needle. The catheter connector has four compo... | 3 | 02/04/2006 | Becton Dickinson & Company |
-