Z-1771-2020 Class II Terminated

Recalled by Acutus Medical Inc — Carlsbad, CA

Recall Details

Product Type
Devices
Report Date
April 29, 2020
Initiation Date
February 25, 2020
Termination Date
April 27, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5 units

Product Description

Acutus Medical AcQGuide Flex Steerable Introducer with AcQcross QX Integrated Dilator/Transseptal Needle, REF: 122852, SterileEO RxOnly

Reason for Recall

It has been determined that the manufacturing process may have left foreign material particulates on the finished device. This could result in a range of event from procedure delay to pulmonary embolism.

Distribution Pattern

US: CA,SC, AZ OUS: None

Code Information

Affected Lot Numbers/Expiration Date: 19101020 /October 2020