Ulnar Osteotomy Compression Plate — Class II medical device recall Z-2877-2018
Terminated recall by TriMed Inc., reported 2018-08-29, distributed in TX. Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wro
| Recall number | Z-2877-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TriMed Inc., Santa Clarita, CA, United States |
| Recall initiated | 2018-04-16 |
| Classified | 2018-08-18 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2021-01-28 |
| Distributed | TX |
| Countries outside the US | AU, CN, SE |
| Quantity | 722 |
| Lot numbers | 10003, 10017 |
Product
Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.
Reason for recall
Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate
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-2877-2018. 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.