Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K043193 |
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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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Totalis, RIGID and Totalis"I Flex ENDO KIT, Manufacturer: C.R. Bard, Inc., Covington, GA 30014. | 2 | 11/14/2016 | C.R. Bard, Inc. |
Bard Inlay Optima® Multi-Length Ureteral Stent Coated Double Pigtail Ureteral Stent with Stent and M... | 2 | 11/14/2016 | C.R. Bard, Inc. |
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