Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K945660 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Autoject EI, REF AJ1310 | 2 | 11/01/2019 | Owen Mumford USA, Inc. |
| Petfine Auto Injector, REF 3310VET | 2 | 11/01/2019 | Owen Mumford USA, Inc. |
| Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an... | 2 | 04/02/2015 | Owen Mumford USA, Inc. |
-







