Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K874063 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Maximal Barrier Drape; Product Codes: ASK-00376-SU | 2 | 05/30/2018 | Arrow International Inc |
| Large Volume Abdominal Paracentesis Kit | 2 | 04/03/2018 | Arrow International Inc |
-







