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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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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2408-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT 2, Product Code IAP-0400 1 06/26/2020 Arrow International Inc
Z-2409-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 SPANISH, Product Code IAP-0400E 1 06/26/2020 Arrow International Inc
Z-2410-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE, Product Code IAP-0500 1 06/26/2020 Arrow International Inc
Z-2411-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE SPANISH, Product Code IAP-0500E 1 06/26/2020 Arrow International Inc
Z-2417-2020 - Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701 1 06/26/2020 Arrow International Inc
Z-2413-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE JAPANESE, Product Code IAP-0500J 1 06/26/2020 Arrow International Inc
Z-2414-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE DUTCH, Product Code IAP-0500NL 1 06/26/2020 Arrow International Inc
Z-2415-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AEROAUTOCAT 2 WAVE, Product Code IAP-0535 1 06/26/2020 Arrow International Inc
Z-2416-2020 - Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/EMEA, Product Code IAP-0700 1 06/26/2020 Arrow International Inc
Z-2412-2020 - Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE ITALIAN, Product Code IAP-0500I 1 06/26/2020 Arrow International Inc
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