Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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Z-1007-2022 - ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery. | 2 | 04/26/2022 | Carl Zeiss Meditec AG |
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