Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2061-2023 — BETTA LINK LG 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: 110045160

U.S. FDA — Device Enforcement · Israel · 2023-05-04 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2061-2023
Date of alert
2023-05-04
Country / jurisdiction
Israel
Risk level
Class II
Risk type
recall
Brand
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10818674025772
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.