Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-0813-2023 - PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0814-2023 - VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0815-2023 - VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0816-2023 - VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0817-2023 - ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0818-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0819-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0820-2023 - ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0821-2023 - ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0822-2023 - ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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