FDAMarch 5, 2025device

stryker Blueprint Mixed Reality Glenoid Box Lid, Catalog Number MRUE205, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

FDA enforcement status: Ongoing

Brands named

tornier s a stornier

UPCs

03700434022971

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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