FDAApril 20, 2018device

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

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

008551060051340085510600514100855106005158008551060051650085510600517200855106005189

Recall history

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

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