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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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Z-2216-2023 - YAMATO PLUS IAB; intra-aortic balloon catheter and accessories used to provide counter pulsation therapy in the aorta. Product Description ... 2 07/21/2023 Datascope Corp.
Z-2217-2023 - SENSATION 7 Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2218-2023 - TRANS-RAY IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Numb... 2 07/21/2023 Datascope Corp.
Z-2219-2023 - MEGA 7.5Fr.IAB , Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2224-2023 - REINFORCED INTRODUCER SET, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2221-2023 - SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2222-2023 - SENSATION PLUS 8Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2223-2023 - LINEAR 7.5Fr.IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
Z-2220-2023 - MEGA 8Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description ... 2 07/21/2023 Datascope Corp.
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