FDAFebruary 25, 2020device

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

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

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

acutus medicalacutus

Recall history

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

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