Tornier S.A.S recalls
Tornier S.A.S has 13 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 14 May 2025. 13 are still ongoing. The most frequent reason is device malfunction.
Total recalls13since 2021
Last 12 months0reported
Class I00% of total
Ongoing13latest 14 May 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 13 100%Class III 0 0%
Why tornier s.a.s is recalled
Product types
By year
Ongoing tornier s.a.s recalls
13 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Blueprint Software, BPUE001. Intended for use by surgeons as a pre recalled | Tornier S.A.S | Device Malfunction | Nationwide |
| Device | CLASS II | stryker Blueprint Mixed Reality Glenoid Box Lid recalled | Tornier S.A.S | Packaging Defects | 7 states |
| Device | CLASS II | stryker HoloBlueprint Application recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Instrument Check Block recalled | Tornier S.A.S | Packaging Defects | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide recalled | Tornier S.A.S | Foreign Material | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Box Base recalled by Tornier S.A.S | Tornier S.A.S | Packaging Defects | 7 states |
All tornier s.a.s recalls, newest first
13 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.