Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K943621 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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remel RapID Yeast Plus System, 20 tests, Ref: R8311007, IVD, containing a 15-ml bottle of RapID Yeas... | 2 | 12/17/2013 | Remel Inc |
ERIC (Electronic RapID Compendium) Version 1.0.77, Catalog Number R8323600, used in conjunction with... | 3 | 02/26/2010 | Remel, Inc |
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