Medical Device Recalls
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1 result found
510(K) Number: K822832 |
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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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BD® Sensi-Disc® Ticarcillin TIC-75, in vitro diagnostic, catalog # 231619, package of 10 cartridges,... | 2 | 03/29/2007 | Becton Dickinson & Co. |
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