Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K910108 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. | 3 | 08/05/2021 | Stanbio Laboratory, LP |
| Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic reagent. | 3 | 08/05/2021 | Stanbio Laboratory, LP |
| Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in vitro diagnostic reagent. | 3 | 08/05/2021 | Stanbio Laboratory, LP |
| Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent. | 3 | 08/05/2021 | Stanbio Laboratory, LP |
| Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent. | 3 | 08/05/2021 | Stanbio Laboratory, LP |
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