# FDA recall Z-3240-2018

> **Stryker GmbH** · Class II · device recall initiated 2018-07-26.

## Product

Hoffmann LRF Hexapod Software   Catalog #:  983031	   Software Version #:   HLRF 1.0-2/002, HLRF 1.1-2/002

## Reason for recall

When creating a correction plan with the  Correct Axial First  button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an erroneously accelerated correction plan for the axial portion of the plan.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-3240-2018
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-26
- **Report date:** 2018-10-03
- **Termination date:** 2020-05-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Selzach, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3240-2018

## Citation

> AI Analytics. FDA recall Z-3240-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-3240-2018. Source: US FDA. Licensed CC0.

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