Think Surgical TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia recall — FDA Z-2716-2026
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
Overview of recall records associated with Think Surgical, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
This page summarizes recall records in which the official source identifies Think Surgical, 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.