Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 12/22/2014 510(K) Number: K974572 |
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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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Gen-Probe AccuProbe Group B Streptococcus Culture Identification Test Kit, 2820. | 1 | 03/10/2011 | Gen-Probe Inc |
Accuprobe Group B Streptococcus Culture Identification Test, Catalog Number 2820B, Batch Number 5313... | 2 | 12/19/2007 | Gen-Probe Inc |
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