FDAFebruary 22, 2016device

Video Duodenoscope

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

The hazard

Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility.

What to do

FDA enforcement status: Terminated

Brands named

pentax medicalpentax

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →