# FDA recall Z-2065-2023

> **T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.** · Class II · device recall initiated 2023-05-04.

## Product

Betta Link LG Reusable Fishmouth 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: 110045157

## Reason for recall

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.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Japan, Netherlands.

## Key facts

- **Recall number:** Z-2065-2023
- **Recalling firm:** T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-04
- **Report date:** 2023-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** GAATON, N/A, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2065-2023

## Citation

> AI Analytics. FDA recall Z-2065-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2065-2023. Source: US FDA. Licensed CC0.

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