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Tornier S.A.S. recalls Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthro
Recalled January 22, 2025 · FDA recall Z-0846-2025 · Tornier S.A.S
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. · FDA Class II
Units
24 units
Sold at
US: MN, KY, MD, MA, TX, AK, TX, ID; France, Canada
Description
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.
Product
Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthroplasty.
Manufacturer(s)
Tornier S.A.S.
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →