Device recall
Z-2065-2023: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone…
FDA device recall · Class II · T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
Key facts
| Recall number (Z-number) | Z-2065-2023 |
|---|---|
| Recall event | 92410 |
| 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 |
| Product code | LXH |
| Recalling firm | T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000272060 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database