Medical Device Recalls
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510(K) Number: K121002 |
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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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| Etest® Ceftaroline (CPT32) WW B30. Etest® (Antimicrobial Susceptibility Testing) is a quantitativ... | 3 | 11/19/2014 | Biomerieux |
| Etest® Ceftaroline (CPT32) WWB100. Etest® (Antimicrobial Susceptibility Testing) is a quantitativ... | 3 | 11/19/2014 | Biomerieux |
| Etest® Ceftaroline (CPT32) US B30. Etest® (Antimicrobial Susceptibility Testing) is a quantitativ... | 3 | 11/19/2014 | Biomerieux |
| Etest® Ceftaroline (CPT32) US B100. Etest® (Antimicrobial Susceptibility Testing) is a quantitati... | 3 | 11/19/2014 | Biomerieux |
| Etest® Ceftaroline (CPT32) US B30. Etest® (Antimicrobial Susceptibility Testing) is a quantitativ... | 3 | 11/19/2014 | Biomerieux |
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