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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Z-1878-2024 - Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS 1 06/03/2024 ARROW INTERNATIONAL Inc.
Z-1880-2024 - Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-05840-U 1 06/03/2024 ARROW INTERNATIONAL Inc.
Z-1879-2024 - Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF IAB-06850-U 1 06/03/2024 ARROW INTERNATIONAL Inc.
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