Medical Device Recalls
-
1 result found
510(K) Number: K133741 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Accu-Chek Performa Test Strip, Blood Glucose Monitoring System, Model number 07299702001 | 2 | 08/26/2021 | Roche Diabetes Care, Inc. |
-