Arrow recalls AutoCAT2 Intra-Aortic Balloon Pumps with serial numbers 160714W-160715W and 160918W due to vibration causing motor connector issues that may lead to pump failure or alarms.
A 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.
Arrow is recalling certain AutoCAT2 Intra-Aortic Balloon Pumps because vibration can damage internal wires, causing pump alarms or sudden failure. This poses a serious risk to patients using the device.
Vibration can cause motor connector wires to fret, char, and discolor. This may trigger pump alarms (System Error 3 and High Baseline) or cause the pump to stop working suddenly.
Patients using the recalled pumps are at risk. Healthcare providers who have the affected models should check their inventory.
Check for serial numbers 160714W through 160715W or 160918W on the pump's label. The product was sold under the Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE DUTCH model.
Immediately stop using the pump if it has a serial number in the range 160714W-160715W or 160918W.
The pump's motor connector wires can fail due to vibration, causing alarms or sudden stoppage of function.
Stop using it immediately and contact Arrow for further instructions.
Yes, the product code is IAP-0500NL with serial numbers 160714W through 160715W and 160918W.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2414-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2414-2020 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
