FDAApril 20, 2018device

LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a. Product Code LS-12; b. Product Code LS-13; c. Product Code LS-14; d. Product Code LS-15; e. Product Code LS-16; f. Product Code LS-17; Laparoscopic, fundic-sparing anti-reflux pro...

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

The hazard

Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or open LINX device.

What to do

FDA enforcement status: Terminated

Brands named

torax medicaltorax

UPCs

008551060050110085510600502800855106005035008551060050420085510600505900855106005066

Recall history

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

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