FDADecember 18, 2024device

Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthroplasty.

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

The hazard

The Pin Guide is being recalled because the metal tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset being unable to detect the Pin Guide and potentially prolonging surgery time or changing of surgical method from guided to conventional.

What to do

FDA enforcement status: Ongoing

Brands named

tornier s a stornier

UPCs

03700434022926

Recall history

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

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