Device 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 pr
Official structured record identifier: 99219.
Publisher
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- July 15, 2026
- Language
- EN
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Official structured record identifier: 99219.
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Source: openFDA Device Recalls
Scope: Regulatory
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