# FDA recall Z-1133-2026

> **MicroPort Orthopedics Inc.** · Class II · device recall initiated 2025-12-19.

## Product

Brand Name: MicroPort  Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE  Model/Catalog Number: HTHT0036  Software Version: N/A  Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLE

## Reason for recall

Due to products not having FDA Premarket authorization to be distributed within the United States.

## Distribution

The product was sent to distributors in multiple US states, including Texas, California, Wisconsin, Kansas, Illinois, Michigan, Tennessee, Maryland, Washington, Georgia, Colorado, Missouri, and Florida.  The product was also sent to the following countries: Belgium, Germany, France, Italy, United Kingdom, Japan, and China.

## Key facts

- **Recall number:** Z-1133-2026
- **Recalling firm:** MicroPort Orthopedics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-19
- **Report date:** 2026-01-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1133-2026

## Citation

> AI Analytics. FDA recall Z-1133-2026. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-1133-2026. Source: US FDA. Licensed CC0.

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