FDA recall Z-0429-2023

ARROW INTERNATIONAL Inc. · Class I · device

Product

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump

Reason for recall

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

Distribution

Worldwide

Key facts

Status: Ongoing
Initiation date: 2022-10-17
Report date: 2022-12-21
Voluntary/Mandated: Voluntary: Firm initiated
Location: Morrisville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0429-2023