NEO SCREW 02 — Class II medical device recall Z-0953-2017
Terminated recall by In2Bones, SAS, reported 2017-01-18, distributed in TN. Dimensional non-conformity of the thread on the screw head.
| Recall number | Z-0953-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | In2Bones, SAS, Ecully, France |
| Recall initiated | 2016-12-19 |
| Classified | 2017-01-06 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2017-02-01 |
| Distributed | TN |
| Countries outside the US | CH, FR |
| Quantity | 40 units |
| Lot numbers | 1604154, 1605083, 1606068 |
| Model numbers | IN2BONES, ST114, W27 |
Product
NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
Reason for recall
Dimensional non-conformity of the thread on the screw head.
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-0953-2017. 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.