Tornier recalls Stry: Blueprint Mixed Reality Glenoid Pin Guide (MRUE200) due to risk of disassembly during surgery, potentially prolonging procedures. Affected units have specific lot numbers.
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.
Tornier is recalling Stryker Blueprint Mixed Reality Glenoid Pin Guides (model MRUE200) because the metal tube might separate from the plastic handle. This could cause the headset to fail during surgery, leading to longer procedures or changes in surgical technique.
The metal tube inside the pin guide can detach from the plastic handle during use. This causes the headset to lose connection with the pin guide, which may lead to longer surgery times or the need to switch from guided to traditional surgical methods.
Surgical teams using the Stryker Blueprint Mixed Reality Glenoid Pin Guide (MRUE200) for total shoulder arthroplasty are most at risk. Patients undergoing this surgery may be affected if the device malfunctions.
Check for the model number MRUE200 on the device. Affected units have lot numbers 22A796, 22A797, 22A978, or 22A979. The product was sold for total shoulder arthroplasty procedures.
Verify if the pin guide's metal tube is securely attached to the plastic handle.
Reach out to Tornier for guidance on next steps if the device is affected.
The device may disassemble during use, which could prolong surgery or require changing surgical methods. Do not use if the metal tube is loose.
Check the lot numbers: 22A796, 22A797, 22A978, or 22A979. Contact Tornier for specific instructions.
Only if the metal tube stays securely attached to the handle. If it disassembles, stop using it immediately.
We’ve drafted a message you can send Tornier to request your refund or repair — edit it as you like.
Subject: Recall Z-0846-2025 — Tornier Tornier Hello, I own a Tornier that is covered by recall Z-0846-2025 from Tornier. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
