FDAApril 20, 2018device

LINX Reflux Management System, Implant Clasp, 13-16 Bead, 1.5T, Product Code LXM-xx, sterile, Rx only. Labeled as: a. Product Code LXM-13; b. Product Code LXM-14; c. Product Code LXM-15; d. Product Code LXM-16; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed wi...

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

00855106005394008551060054000085510600541700855106005424

Recall history

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

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