Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053559 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Gen-Probe LIFECODES PF4 Enhanced assay, Catalog No. X-HAT45 GTI PF4 Enhanced is designed as a sol... | 2 | 03/28/2013 |
FEI # 2183608 Genetic Testing Institute,inc |
| PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIF... | 2 | 01/20/2015 |
FEI # 2183608 Genetic Testing Institute,inc |
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