Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K121002 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
-