Synthes VA Implant Rack for the Compact Distal Radius System… — Class II medical device recall Z-0867-2017
Terminated recall by Synthes (USA) Products LLC, reported 2016-12-28, distributed nationwide. The screw rack plate was assembled incorrectly which could cause the screws in the screw rack to sit low and t
| Recall number | Z-0867-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthes (USA) Products LLC, West Chester, PA, United States |
| Recall initiated | 2016-11-29 |
| Classified | 2016-12-21 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2017-08-03 |
| Distributed | Nationwide (US) |
| Quantity | 31 units |
| Lot numbers | FL00528 |
| Model numbers | 60.119.012 |
Product
Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument
Reason for recall
The screw rack plate was assembled incorrectly which could cause the screws in the screw rack to sit low and touch the surface beneath the screw rack.
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-0867-2017. 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.