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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 16 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
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Z-0009-2024 - Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0024-2024 - Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE, Catalog number M003101630, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0011-2024 - Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM, Catalog number H965100440, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0012-2024 - Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE, Catalog number H965100460, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0013-2024 - Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE, Catalog number H965100470, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0014-2024 - Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE, Catalog number H965100480, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0015-2024 - Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM, Catalog number M003100620, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0016-2024 - Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE, Catalog number M003100630, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0017-2024 - Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM, Catalog number M003101420, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
Z-0018-2024 - Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM, Catalog number M003101430, cardiac guide catheter 2 10/03/2023 Boston Scientific Corporation
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