# FDA recall Z-0110-2022

> **Uoc Usa Inc** · Class II · device recall initiated 2021-08-27.

## Product

United Orthopedics USTAR II Knee System    USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025

## Reason for recall

Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.

## Distribution

U.S. Nationwide:  CA, CO, and NV    No O.U.S.

## Key facts

- **Recall number:** Z-0110-2022
- **Recalling firm:** Uoc Usa Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-27
- **Report date:** 2021-10-20
- **Termination date:** 2023-01-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0110-2022

## Citation

> AI Analytics. FDA recall Z-0110-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0110-2022. Source: US FDA. Licensed CC0.

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