FDAJanuary 22, 2016device

3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.

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

The hazard

3M discovered a valve with incorrectly labeled "input" and "output" orientation. This defect can result in the valve being installed backwards, creating a remote possibility of valve failure. A failure may result in EO being vented outside the sealed chamber during a limited period in the EO injection phase of the cycle.

What to do

FDA enforcement status: Terminated

Brands named

3m company health care business

Recall history

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

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3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL. — Recall Details · AllClear