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FDAOctober 17, 2022device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

What to do

FDA enforcement status: Ongoing

Brands named

arrow

UPCs

0080190204341230801902043413

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump — Recall Details · AllClear