Arrow recalls AutoCAT2 Intra-Aortic Balloon Pumps with serial numbers 140868V-191148V due to vibration causing motor connector issues that may lead to pump alarms or failure.
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 AutoCAT2 Intra-Aortic Balloon Pumps with specific serial numbers because a component can fail from vibration, causing pump alarms or sudden stoppage. This could be dangerous for patients using the device.
Vibration can cause the motor connector wires to fret, char, and discolor. This may trigger pump alarms like System Error 3 or High Baseline, and could lead to sudden pump failure or inability to start the device.
Patients using the recalled AutoCAT2 pumps are at risk. Medical professionals who have the device in their care may need to take action if they own the affected serial numbers.
Check the serial number on the pump. The affected models have serial numbers ranging from 140868V through 191148V as listed in the recall notice.
Identify the serial number on your pump to see if it falls within the listed ranges (140868V through 191148V).
The recalled model is Arrow AutoCAT2 Intra-Aortic Balloon Pump with Product Code IAP-0400.
The pump may show alarms like System Error 3 or High Baseline, or it could stop working suddenly.
Check the serial number on the pump. Affected models have serial numbers from 140868V through 191148V as listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2408-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2408-2020 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.
