Medical Device Recalls
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1 result found
510(K) Number: K010401 |
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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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Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile.... | 2 | 08/16/2005 | Medical Device Group Inc. |
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