Tornier recalls Blueprint Mixed Reality Instrument Kit (MRUEGLN) for software and instrument issues affecting total shoulder arthroplasty procedures. Affected units sold from Aug 2023 to Dec 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 Instrument Kit for total shoulder arthroplasty procedures due to reported difficulties with software and instrument functionality. This could prevent the system from working as intended during surgery.
The system has been reported to have software and instrument issues that prevent it from functioning properly during surgery. These problems could lead to difficulties in using the product as intended for total shoulder arthroplasty procedures.
Surgical teams using the Blueprint Mixed Reality Instrument Kit for total shoulder arthroplasty procedures are affected. Surgeons and surgical staff who purchased the kit between August 2023 and December 2024 are most at risk.
Check for the catalog number MRUEGLN on the instrument kit. The product was sold from August 2023 through December 2024 for total shoulder arthroplasty procedures.
Look for the catalog number MRUEGLN on the instrument kit.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system, which prevents it from meeting its intended use.
The catalog number is MRUEGLN.
The product was distributed from August 2023 through December 2024.
We’ve drafted a message you can send Tornier to request your refund or repair — edit it as you like.
Subject: Recall Z-1541-2025 — Tornier Tornier Hello, I own a Tornier that is covered by recall Z-1541-2025 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.
