Medical Device Recalls
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1 result found
510(K) Number: K092745 |
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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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100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to eth... | 3 | 09/06/2012 | Steris Corporation |
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