# FDA recall Z-1738-2025

> **Tornier S.A.S.** · Class II · device recall initiated 2025-04-10.

## Product

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

## Reason for recall

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

## Distribution

Blueprint Version 4.2.1 is only currently available in the US. Domestic distribution nationwide.

## Key facts

- **Recall number:** Z-1738-2025
- **Recalling firm:** Tornier S.A.S.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-10
- **Report date:** 2025-05-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Montbonnot-Saint-Martin, N/A, France

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1738-2025

## Citation

> AI Analytics. FDA recall Z-1738-2025. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-1738-2025. Source: US FDA. Licensed CC0.

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