Reported Jan 22, 2025 · Ongoing
Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder…
Tornier S.A.S.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Tornier S.A.S. · 161 Rue Lavoisier · Montbonnot-Saint-Martin · N/A
Is this the product you have?
- Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthroplasty.
- Lot codes and dates
- UDI/DI 03700434022926
- Lot Numbers
22A79622A79722A978and 22A979
- Amount recalled
- 24 units
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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