Reported Jul 12, 2023 · Ongoing
BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural…
T.a.g. Medical Products Corporation, Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. · Kibbutz Gatton · GAATON, N/A · N/A
Is this the product you have?
- 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 Number110045154
- Lot codes and dates
- UDI-DI0818674025765
- Lot Numbers
21R0121R0221R0322C0222C0322C0622C0822E0122E0222F0122F0222F0322J0122J0222J0322K0122K0222K0322K0422K0522K0722K0822K0922K1022K1122M0122M0222M0322M0422N0122P0122P0222P0322P0422P0522R01
- Amount recalled
- N/A
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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