Gridlock Ankle Screw Driver Bit REF 320-35-003 — Class II medical device recall Z-0799-2020
Terminated recall by Trilliant Surgical, LLC, reported 2020-01-22, distributed nationwide. A screwdriver used to facilitate implant insertion and removal was found to be out of specification for the mi
| Recall number | Z-0799-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trilliant Surgical, LLC, Houston, TX, United States |
| Recall initiated | 2019-03-14 |
| Classified | 2020-01-10 |
| Reported by FDA | 2020-01-22 |
| Terminated | 2022-03-16 |
| Distributed | Nationwide (US) |
| Quantity | 20 units |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00812926026893 |
| Lot numbers | TSL006617 |
| Model numbers | 320-35-003 |
Product
Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.
Reason for recall
A screwdriver used to facilitate implant insertion and removal was found to be out of specification for the minor diameter of the drive feature causing the driver to be unable to retain screws as intended.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0799-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.