Medical Device Recalls
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1 result found
510(K) Number: K141693 |
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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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Tyvek Pouch/Roll with STERRAD Chemical Indicator, P/N 12425 | 2 | 03/23/2015 | Advanced Sterilization Products |
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