Medical Device Recalls
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1 result found
510(K) Number: K072759 |
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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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| Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only | 1 | 01/28/2019 |
FEI # 3000223297 WEST PHARMA. SERVICES IL, LTD |
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