Medical Device Recalls
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1 result found
510(K) Number: K082211 |
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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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***REF 66800694***Qty 10***smith&nephew***RENASYS Port Foam Dressing Kit Port***STERILE***Rx Only.**... | 2 | 01/26/2012 | Smith & Nephew Inc. |
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