Medical Device Recalls
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1 result found
510(K) Number: K932855 |
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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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Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage... | 2 | 03/26/2021 | Hollister Incorporated |
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