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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2626-2026 - CRE Pro Wireguided 6-8mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2627-2026 - CRE Pro Wireguided 8-10mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2628-2026 - CRE Pro Wireguided 10-12mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2629-2026 - CRE Pro Wireguided 12-15mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2630-2026 - CRE Pro Wireguided 15-18mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2637-2026 - CRE Wireguided 18-20mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2632-2026 - CRE Wireguided 6-8mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2633-2026 - CRE Wireguided 8-10mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2634-2026 - CRE Wireguided 10-12mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
Z-2635-2026 - CRE Wireguided 12-15mm 240cm 2 07/01/2026 FEI # 3005099803
Boston Scientific Corporation
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