FDAMay 4, 2023device

Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156

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

The hazard

Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.

What to do

FDA enforcement status: Ongoing

Brands named

t a g medical products

UPCs

10818674025819

Recall history

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

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Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156 — Recall Details · AllClear