Medical Device Recalls
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1 result found
510(K) Number: K133968 |
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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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Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sa... | 2 | 08/26/2022 | Mckesson Medical-Surgical Inc. Corporate Office |
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