Medical Device Recalls
-
1 result found
510(K) Number: K072443 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VITROS® Chemistry Products CDM PROM Calibration Data Module Rev. No. 0168 and 0169 (Product Code 199... | 2 | 08/13/2014 | Ortho-Clinical Diagnostics |
-