Class II

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

Tornier S.A.S. · December 18, 2024

Reason for Recall

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.

Distribution

US: MN, KY, MD, MA, TX, AK, TX, ID; France, Canada

States Affected

AK, ID, KY, MA, MD, MN, TX

Quantity Affected

24 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0846-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Tornier S.A.S. Medical Device Recall: Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthroplasty. | SafeCheck