Arrow International Inc: Medical Device Recall in 2020 - (Recall #: Z-2414-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE DUTCH, Product Code IAP-0500NL

Product Classification:

Class I

Date Initiated: May 20, 2020

Date Posted: July 8, 2020

Recall Number: Z-2414-2020

Event ID: 85684

Reason for Recall:

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.

Status: Terminated

Product Quantity: 2123 total

Code Information:

Serial Number Ranges: 160714W through 160715W 160918W

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated