Official recall record
stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder Arthroplasty
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-03-05
- Country of alert
- France
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 03700434022988
- Brand on record
- Tornier S.A.S.
What the authority reported
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-03-05 · US FDA — Medical Devices
stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Re - 2025-03-05 · US FDA — Medical Devices
stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed - 2025-03-05 · US FDA — Medical Devices
stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
All 5 official recall notices naming Tornier S.A.S. on this site →
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