Medical Device Recalls
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1 result found
510(K) Number: K951295 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tyvek Self-Seal Pouch with STERRAD Chemical Indicator 12332. Intended to be used to contain medic... | 2 | 02/22/2011 |
FEI # 3003662624 Advanced Sterilization Products |
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