FDADecember 22, 2022device

Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0 50205 3.0 50305 4.0 50405

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

The hazard

There is an orogastric (OG) tube size discrepancy between the labeling in the IFU and the printed text on the device. If the clinician is unable to pass a gastric catheter through one of the channels, the clinician may use a smaller-diameter gastric catheter.

What to do

FDA enforcement status: Ongoing

Brands named

sunmed

UPCs

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Recall history

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

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