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FDA
Food and Drug Administration · Recall Z-2716-2026 · May 8, 2026

TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing softwar

Think Surgical, Inc.

The hazard

Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.