Medical Device Recalls
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1 result found
510(K) Number: K003395 |
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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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APTIMA Urine Collection Kit; Catalog Number 301040, Lots 27231, 27232, 27233, and 27234. Produc... | 3 | 06/14/2014 | Gen-Probe Inc |
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