FDAMarch 21, 2022device

Avanos Cortrak 2 Enteral Access System (EAS)

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

The hazard

Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.

What to do

FDA enforcement status: Terminated

Brands named

avanos medicalavanos

UPCs

00350770472010003507704720651068065147201110680651472066

Recall history

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

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