Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K023487 |
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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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| CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-cou... | 3 | 09/23/2020 |
FEI # 3004142665 OraSure Technologies, Inc. |
| Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage:... | 3 | 09/23/2020 |
FEI # 3004142665 OraSure Technologies, Inc. |
| Personelle OTC Skin Tag Remover, Canada Catalog Number: 1001-0314 - Product Usage: indicated for o... | 3 | 09/23/2020 |
FEI # 3004142665 OraSure Technologies, Inc. |
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