FDAOctober 10, 2022device

CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit

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

The hazard

An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.

What to do

FDA enforcement status: Terminated

Brands named

caire

Recall history

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

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