The DARCO¿ Locking Bone Plate System is designed with rhombus — Class II medical device recall Z-0679-2022
Terminated recall by Wright Medical Technology, Inc., reported 2022-03-09. Product was labelled with the incorrect manufacturing and distribution dates.
| Recall number | Z-0679-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2022-02-09 |
| Classified | 2022-02-25 |
| Reported by FDA | 2022-03-09 |
| Terminated | 2024-01-25 |
| Countries outside the US | GB, JP |
| Quantity | 12 units |
| Lot numbers | 11012187061566009 |
| Model numbers | DCS2825126 |
Product
The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or 3.5mm screws which intersect each other in pairs. The drill holes of the plates are aligned to assure the screws do not touch. The various plates model numbers differ from each other through among other things different curvatures, material strengths, lengths, number of plate holes and through different grades and bridge widths
Reason for recall
Product was labelled with the incorrect manufacturing and distribution dates.
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-0679-2022. 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.