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
Reported: January 28, 2026 Initiated: December 19, 2025 #Z-1133-2026
Product Description
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.
Details
- Recalling Firm
- MicroPort Orthopedics Inc.
- Units Affected
- 91
- 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.
- Location
- Arlington, TN
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by MicroPort Orthopedics Inc.. Units affected: 91.
Why was this product recalled? ▼
Due to products not having FDA Premarket authorization to be distributed within the United States.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 28, 2026. Severity: Moderate. Recall number: Z-1133-2026.
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