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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 16 of 16 Results
Related Medical Device Recalls
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Product Description
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Z-0019-2024 - Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM, Catalog number M003101440, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0020-2024 - Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE, Catalog number M003101460, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0021-2024 - Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE, Catalog number M003101470, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0022-2024 - Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE, Catalog number M003101480, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0023-2024 - Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM, Catalog number M003101620, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0010-2024 - Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM, Catalog number H965100430, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
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