Tornier S.A.S. recalls
Every recall we track for Tornier S.A.S. — 13 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Tornier S.A.S. more than tripled in 2025 (10, up from 2 in 2024).
All FDA recall records for Tornier S.A.S. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 1 | 0 | 2 |
| 2025 | 0 | 0 | 10 | 0 | 10 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Tornier S.A.S. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Tornier S.A.S. recalls
5 shown- Lower riskMedical device
Tornier S.A.S. recalls Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
Tornier recalls Blueprint software version 4.2.1 for surgeons due to incompatibility with older cases. This affects shoulder replacement planning software.
TornierApr 10, 2025 - Lower riskMedical device
Tornier S.A.S. recalls stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality
Tornier recalls Blueprint Mixed Reality Coracoid Clamps (MRUE202) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
TornierMar 5, 2025 - Use cautionMedical device
Tornier S.A.S. recalls Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder
Tornier recalls Stry: Blueprint Mixed Reality Glenoid Pin Guide (MRUE200) due to risk of disassembly during surgery, potentially prolonging procedures. Affected units have specific lot numbers.
TornierDec 18, 2024 - Lower riskMedical device
Tornier S.A.S. recalls Stryker Blueprint Software, Catalog #BPUE001.
Tornier recalls Stryker Blueprint Software versions 2.1.4 to 4.0.2 due to incompatible implant configurations that lack regulatory approval. Affected units have specific UDI-DI numbers.
TornierApr 16, 2024 - Lower riskMedical device
Tornier S.A.S. recalls The Aequalis Pyrocarbon Humeral Heads. Shoulder implant component. Sold OUS only: a) Catalog # DWH039 - Diameter 39 mm
Tornier recalls specific shoulder implant components (Aequalis Pyrocarbon Humeral Heads) due to potential graphite exposure. Affected models include catalog numbers DWH039 to DWH154 with varying diameters and heights. Consumers should check their implant details and contact Tornier for guidance.
TornierJun 25, 2021
Tornier S.A.S. recall questions
How many recalls has Tornier S.A.S. had?
13 recalls from Tornier S.A.S. are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Tornier S.A.S. recall?
Tornier S.A.S. recalls Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement., dated Apr 10, 2025. Every Tornier S.A.S. recall is listed on this page, newest first.
What should I do if I have a recalled Tornier S.A.S. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Tornier S.A.S. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.