# FDA recall Z-1217-2024

> **United Orthopedic Corporation** · Class II · device recall initiated 2024-01-03.

## Product

USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers:    REF: PE25153109 -  PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm,  PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211 - 11X150, PE25151213 - 13X150mm, PE25151215 - 15X150mm, PE25151217 - 17X150mm, PE25151415 - 15x200mm

## Reason for recall

Their is a potential that the implant curved stem  may be oriented incorrectly.

## Distribution

US: CA,KY, MI, IN, TN, CO, FL, TX, NV,  OUS: Switzerland, United Kingdom, Malaysia, Philippines, Taiwan

## Key facts

- **Recall number:** Z-1217-2024
- **Recalling firm:** United Orthopedic Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-03
- **Report date:** 2024-03-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hsinchu, Taiwan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1217-2024

## Citation

> AI Analytics. FDA recall Z-1217-2024. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-1217-2024. Source: US FDA. Licensed CC0.

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