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Recall Observatory FDA recall evidence

Device 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

Z-1133-2026

December 19, 2025

Class II

Product summary

Firm
MicroPort Orthopedics Inc.
Event
Event 98220
Status
Ongoing
Classification
Class II
Quantity
91
Official record key
device-enforcement:Z-1133-2026

Official wording

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

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

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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