Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Due to Drill guides might bend when axial forces are...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. directly.
Affected Products
BETTA LINK SR KNOTLESS IMPLANT KIT-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:110045154
Quantity: N/A
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report