DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes… — Class II medical device recall Z-2816-2020
Terminated recall by Synthes (USA) Products LLC, reported 2020-08-26, distributed nationwide. May have one or more dimensional features out of tolerance includes: thread pitch diameter depth, thread minor
| Recall number | Z-2816-2020 |
|---|---|
| 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 | 2020-07-21 |
| Classified | 2020-08-17 |
| Reported by FDA | 2020-08-26 |
| Terminated | 2022-02-18 |
| Distributed | Nationwide (US) |
| Quantity | 191 units |
| Reason classes | potency |
| UPC / GTIN / UDI-DI | 10886982166913 |
| Lot numbers | 29P6036 |
| Model numbers | 241.381 |
Product
DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes / 93mm - Product Usage: intended for fixation of fractures, osteotomies and non-unions of clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, distal tibia and fibula, particularly in osteopenic bone. Part Number 241.381
Reason for recall
May have one or more dimensional features out of tolerance includes: thread pitch diameter depth, thread minor diameter depth, plate thickness and end length out of tolerance that can potentially result in a reduced locking strength of an LCP screw
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-2816-2020. 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.