ClearanceBrief
Recall Z-0446-2023 ยท DSP System, Balloon, Intra-Aortic And Control

ARROW INTERNATIONAL Inc.

Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump

DateDec 15, 2022 (initiated Oct 17, 2022)
StatusOpen, Classified
ReasonThere is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Root causePending
ActionThe firm issued an URGENT MEDICAL DEVICE NOTIFICATION to its consignees on 10/17/2022 by FedEx 2-day mail. To reduce the risk of short battery run time: .Plug IABP into an AC outlet during patient use, and when not in use. .Ensure the battery is fully charged prior to transporting patients, and a fully charged backup IABP device is available. .Replace the batteries when Battery Run Time is less than 90 minutes, there is visual damage to the battery, or Battery has been in service for 3 years. . Perform Battery Load Test at least every 12 months by qualified service personnel. If t
Quantity4 units
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K060309AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES
Arrow Intl., Inc., Apr 6, 2006