# FDA recall Z-2816-2020

> **Synthes (USA) Products LLC** · Class II · device recall initiated 2020-07-21.

## 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

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2816-2020
- **Recalling firm:** Synthes (USA) Products LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-21
- **Report date:** 2020-08-26
- **Termination date:** 2022-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Chester, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2816-2020

## Citation

> AI Analytics. FDA recall Z-2816-2020. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-2816-2020. Source: US FDA. Licensed CC0.

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