FDAAugust 4, 2015device

Angiographic Injector. Medrad Mark 7 Arterion Injection System, which utilizes Software Version SW 005.006_SH; to be used specifically for the purposes of injecting contrast medium and common flushing solutions into humans for angiographic studies.

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

The hazard

Software Version SW 005.006_SH, resulted in the removal of purge enforcement from traditional New-Case, Power Up and Syringe Change use cases while the injector head is in the upright position.

What to do

FDA enforcement status: Terminated

Brands named

bayer healthcarebayer

Recall history

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

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