Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K033009 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Albumin Gen.2, Catalog 05166861190 | 3 | 10/13/2020 | Roche Diagnostics Operations, Inc. |
Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro... | 3 | 10/16/2019 | Roche Diagnostics Operations, Inc. |
Roche Diagnostics ALBT2, Tina-quant Albumin Gen. 2, COBAS INTEGRA, cobas c systems, Roche Diagnostic... | 2 | 10/09/2008 | Roche Diagnostics Corp. |
-