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Arrow International Inc Recall: Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IA

Arrow International Inc Recall: Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IA is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Arrow International Inc; Product: Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701; Reason for recall: A

Recalling firmArrow International Inc
ProductArrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701
Reason for recallA potential issue with a component within the above-referenced IABPs may impact the ability of the devices to operate. A Component within the IABP is susceptible to vibration failure resulting in fretting, charring, and discoloration of motor connector wires, which may result in pump alarms for System Error 3 and High Baseline presented on the screen of the IABP, and potential abrupt cessation of function or inability to start the IABP.
ClassificationClass I (most serious — reasonable probability of serious health consequences or death)
StatusTerminated
DistributionWorldwide distribution.
Recall initiated20200520
Recall numberZ-2417-2020
Categorydevice
StatePA
CountryUnited States

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