Medical Device Recalls
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1 result found
510(K) Number: K883427 |
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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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Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests. ... | 3 | 09/24/2012 | Clark Laboratories, Inc. (dba,Trinity Biotech USA) |
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