Medical Device Recalls
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1 result found
510(K) Number: K984136 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bardex® Foley Catheter, 22 Fr 40cc- 20cc Ribbed Balloons, Coleman Model Red Latex, 3 Way Radiopaque,... | 3 | 08/21/2003 | C.R. Bard, Inc., Urological Division |
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