# FDA recall Z-1215-2024

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

## Product

USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers:  REF: PE11151211 -  11x150mm,	PE11151213 -  13x150mm, 	PE11151215 - 15x150mm,	PE11151217 - 17x150mm,	PE11151411 - 11x200mm,	PE11151413 - 13x200mm,	PE11151415 - 15x200mm,	PE11151417 - 17x200mm,

## 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-1215-2024
- **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-1215-2024

## Citation

> AI Analytics. FDA recall Z-1215-2024. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-1215-2024. Source: US FDA. Licensed CC0.

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