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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 31 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0446-2023 - Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0447-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500D (IPN000321), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0448-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500E (IPN000322), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0449-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500EX (IPN000322), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0450-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500F (IPN000323), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0451-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500I (IPN000324), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0452-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000325), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0453-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500NL (IPN000326), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0454-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500SV (IPN000327), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
Z-0455-2023 - Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump 1 12/15/2022 ARROW INTERNATIONAL Inc.
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