Tornier Blueprint Software 4.2.1 Recall: Incompatible Previous Cases

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Recalling firmTornier S.A.S.161 Rue Lavoisier, N/A · Montbonnot-Saint-Martin, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Tornier is recalling its Blueprint software version 4.2.1 for surgeons who use it to plan shoulder replacements. The software bug prevents accessing cases from previous versions, which could lead to errors in surgical planning.

Why it’s dangerous

The software bug in version 4.2.1 prevents users from accessing cases created in previous versions. This could cause errors in surgical planning if surgeons try to use older cases in the new software.

Who’s affected

Surgeons who use Tornier's Blueprint software for shoulder replacement planning are affected. Those who have cases from older software versions are most at risk.

How to tell if you have this one

Check if you have Blueprint software version 4.2.1 for shoulder replacement planning. The software was intended for surgeons and sold as BPUE001.

Brand
Tornier
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify your Blueprint software version by checking the software's version number or documentation.

✎ GovInfoNow

Questions people ask

Why is this software being recalled?

The software bug in version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.

What should I do if I have this software?

Check your software version. If you have version 4.2.1, you may need to update or contact Tornier for assistance.

Is there a fix available?

The recall record does not specify a remedy or fix.

Take action

Contact Tornier

We’ve drafted a message you can send Tornier to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1738-2025 — Tornier Tornier

Hello,

I own a Tornier that is covered by recall Z-1738-2025 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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Where this comes from

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.

Official source: FDA Recall #Z-1738-2025 (April 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1738-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Tornier S.A.S. recalls Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.

Lower-risk recall