Medical Device Recalls
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71 to 80 of 94 Results
Related Medical Device Recalls |
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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|---|---|---|---|
| Z-0822-2023 - ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0851-2023 - ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0863-2023 - ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348 | 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-0841-2023 - ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0846-2023 - ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046 | 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-0819-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252 | 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-0817-2023 - ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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