Tornier recalls Blueprint Mixed Reality Glenoid Box Lids (MRUE205) due to software and instrumentation problems affecting shoulder surgery. Affected units were sold from August 2023 to December 2024.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Tornier is recalling its Blueprint Mixed Reality Glenoid Box Lids (model MRUE205) because they cause software and hardware issues that prevent the device from working properly during shoulder surgery. This could lead to difficulties in the surgical procedure.
The device has software and hardware issues that prevent it from meeting its intended use during shoulder surgery. These problems can cause difficulties in the surgical procedure, but do not typically cause serious injury.
Surgical teams using the Tornier Blueprint Mixed Reality Glenoid Box Lids for shoulder replacements are affected. Patients undergoing these surgeries may be at risk if the device doesn't function correctly.
Check for the catalog number MRUE205 on the Glenoid Box Lid. The product was sold from August 2023 through December 2024 in packages labeled 'Tornier Blueprint Mixed Reality'.
Look for the catalog number MRUE205 on the Glenoid Box Lid.
Tornier identified an elevated complaint rate related to software and instrumentation issues that prevent the device from meeting its intended use during shoulder surgery.
The recall record does not specify a remedy, so check the product details to see if it matches the catalog number MRUE205.
The recall indicates software and instrumentation issues that could cause difficulties in surgery, but the hazard level is low risk as it does not typically cause serious injury.
We’ve drafted a message you can send Tornier to request your refund or repair — edit it as you like.
Subject: Recall Z-1539-2025 — Tornier Tornier Hello, I own a Tornier that is covered by recall Z-1539-2025 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.
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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.
