Medical Device Recalls
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1 result found
510(K) Number: K092488 |
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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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DYNAREX DynaLube LUBRICATING JELLY, STR 2.7GM (144/BX 12BX/CS) Catalog #1250 | 2 | 08/26/2022 | Mckesson Medical-Surgical Inc. Corporate Office |
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