Medical Device Recalls
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1 result found
510(K) Number: K021736 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bard®Ventralex" Hernia Patch Medium Circle with Strap Diameter 6.4cm /2.5",\ Catalog #0010302, l... | 2 | 05/02/2011 | Davol, Inc., Sub. C. R. Bard, Inc. |
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