Recall
FDAHealthDecember 19, 2025

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

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

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
December 19, 2025

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.

What's affected?

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
Lot code
Part

Additional details

Lot Code: Part Number HTHT0036, all lots, no future lots planned. Primary DI Number 00192629320130. Secondary Device ID M684HTHT00361

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 91.

View original FDA notice →

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