Medical Device Recalls
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1 result found
Recall Number: Z-1722-2018 |
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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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| BEQ-T 25502 1/4 Better Bladder , Custom Tubing Kit, Catalog No. 709000434 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
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