FDADecember 22, 2022device

AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size REF Number 0.0 60005 0.5 60055 1.0 60105 1.5 60155 2.0 60205 3.0 60305 4.0 60405

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

008149540202631081495402026000814954020270108149540202770081495402028710814954021083008149540202941081495402109000814954020300108149540211060081495402031710814954021113

Recall history

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

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AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size REF Number 0.0 60005 0.5 60055 1.0 60105 1.5 60155 2.0 60205 3.0 60305 4.0 60405 — Recall Details · AllClear