Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K163513 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH | 2 | 01/22/2020 | Arrow International Inc |
ARROW Endurance Extended Dwell Peripheral Catheter System | 1 | 06/21/2023 | ARROW INTERNATIONAL Inc. |
-