7 Hole VL Gridlock Fibula Plate — Class II medical device recall Z-2490-2015
Terminated recall by Trilliant Surgical Ltd., reported 2015-09-09, distributed in CA, FL, MN, NJ, NM, OH, WI. The affected parts subject to the recall are out of specification, resulting in in the loss of the optimal loc
| Recall number | Z-2490-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trilliant Surgical Ltd., Houston, TX, United States |
| Recall initiated | 2015-08-06 |
| Classified | 2015-08-31 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2017-01-26 |
| Distributed | CA, FL, MN, NJ, NM, OH, WI |
| Quantity | 28 units |
| Reason classes | specification failure |
| Lot numbers | TSL002595, TSL002596, TSL002597 |
| Model numbers | 300-60-001, 300-60-002, 300-60-003 |
Product
7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part # 300-60-002 NON-STERILE SINGLE USE ONLY; 11 Hole VL Gridlock Fibula Plate, Part # 300-60-003 NON-STERILE SINGLE USE ONLY. For use in trauma and reconstructive procedures in small bones.
Reason for recall
The affected parts subject to the recall are out of specification, resulting in in the loss of the optimal locking screw functionality of the plates. The thread depth of the screw holes is insufficient, potentially limiting the ability to engage and lock with associated mating locking screws.
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-2490-2015. 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.