FDAApril 25, 2024device

EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only

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

The hazard

Due to saline conductivity issues, their is a potential that dilation catheters may provide inaccurate esophageal diameter measurements that may lead to various harms.

What to do

FDA enforcement status: Ongoing

Brands named

covidien

UPCs

1088452180945120884521809458

Recall history

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

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EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only — Recall Details · AllClear