Reported May 14, 2025 · Ongoing
Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
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 · N/A
Is this the product you have?
- Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
- Lot codes and dates
- Software Version 4.2.1
- Amount recalled
- 438 users
Where it was sold
- Nationwide
Why it was recalled
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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