Medical Device Recalls
-
|
1 result found
510(K) Number: K874425 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| BD BBL Sensi Disc Ciprofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. C... | 2 | 02/08/2024 | Becton Dickinson & Co. |
-







