ProductGuru Recalls

Official recall record

stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog

US FDA — Medical Devices · 2025-03-05 · FranceClass II
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)
03700434022940
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.

More recalls: US FDA — Medical Devices · France · all filters

Other recalls from this brand

All 5 official recall notices naming Tornier S.A.S. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.