Medical DeviceJan 28, 2026
MicroPort HIPTURN FEM HEAD TRIAL 36MM REUSABLE recall — FDA Z-1133-2026
Due to products not having FDA Premarket authorization to be distributed within the United States.
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies MicroPort Orthopedics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.