FDAOctober 11, 2017device

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

The hazard

Possible incomplete seal between the CO2 absorber and the breathing circuit CO2 bypass port assembly of the Carestation 600 Series systems.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems china

UPCs

101296200001012965000010129655000101296500021012962000210129655002

Recall history

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

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