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T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. recalls Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural lig

Recalled July 12, 2023 · FDA recall Z-2064-2023 · T.A.G. MEDICAL PRODUCTS

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. · FDA Class II
Units
N/A
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Japan, Netherlands.

Description

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.

Product
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
Manufacturer(s)
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
Made in
Israel

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. recalls Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural lig | RecallWatchUSA