Medical Device Recalls
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1 result found
Recall Number: Z-1071-2025 |
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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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| Olympus Single Use Guide Sheath Kits with the following product descriptions and model numbers: 1... | 1 | 02/11/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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