Brand

Tornier S.A.S.: official recall notices

5 official recall or safety notices on this site name Tornier S.A.S., dated 2025-03-05. They were issued by 1 authority: US FDA — Medical Devices (5).

Countries where the notices were issued: France (5).

Name as written in the notices: Tornier S.A.S.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

Year	Notices
2025	5

Notices by authority

Authority	Notices
US FDA — Medical Devices	5

All notices

Date	Authority	Product	Hazard (as classified)
2025-03-05	US FDA — Medical Devices	stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality Inst	—
2025-03-05	US FDA — Medical Devices	stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed Reality I	—
2025-03-05	US FDA — Medical Devices	stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder Arthroplasty	—
2025-03-05	US FDA — Medical Devices	stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty	—
2025-03-05	US FDA — Medical Devices	stryker Blueprint Mixed Reality Box Base, Catalog Number MRUE204, packaged in stryker Blueprint Mixed Reality Instrument	—

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