Medical Device Recalls
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1 result found
510(K) Number: K162508 |
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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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3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158 | 3 | 09/26/2022 | Mckesson Medical-Surgical Inc. Corporate Office |
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