Home / Brands / ARROW INTERNATIONAL
ARROW INTERNATIONAL Recalls
525 recalls on record · June 27, 2012 to June 24, 2026 · Medical Devices
Recalls by year
12
13
14
15
16
17
18
19
20
21
22
23
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500SV (IPN000327), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500NL (IPN000326), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000325), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500I (IPN000324), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500F (IPN000323), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500EX (IPN000322), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500E (IPN000322), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500D (IPN000321), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400E (IPN000305), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN917286), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN916549), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN001113), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus REFURBISHED, REF IAP-0700X (IPN914274), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700 (IPN001112), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN917288), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN916548), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601 (IPN001109), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN917287), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN001108), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2 WAVE REFURBISHED, REF IAP-0535X (IPN000329), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT 2 WAVE, REF IAP-0535 (IPN000329), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE REFURBISHED, REF IAP-0500X (IPN000328), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2, REF IAP-0435 (IPN000312), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 IAPB, REFURBISHED, REF IAP-0400X (IPN000311), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
December 21, 2022Medical DevicesFDA
ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB, REF IAP-0400 (IPN000302), cardiac pump
Hazard: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.