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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-3146-2026
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Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS); 2 09/11/2026 FEI # 3009507273
Maquet Cardiopulmonary Gmbh
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