Medical Device Recalls
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1 result found
510(K) Number: K811269 |
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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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| Vial Decanter, REF 2006S. Packaged on a form, fill and seal machine with a poly/Tyvek material then ... | 2 | 08/16/2024 |
FEI # 3014342658 Microtek Medical Inc. |
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