Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131544 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Bilirubin Total Gen.3, Cat. Nos. 05795397190, 05795419190, 05795320160, 05795338160, 05795346160 ... | 2 | 04/13/2019 |
FEI # 1823260 Roche Diagnostics Corporation |
| Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the qu... | 3 | 10/16/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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