Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #:… — Class II medical device recall Z-3240-2018
Terminated recall by Stryker GmbH, reported 2018-10-03, distributed nationwide. When creating a correction plan with the Correct Axial First button selected and the No. of corrections per da
| Recall number | Z-3240-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, Switzerland |
| Recall initiated | 2018-07-26 |
| Classified | 2018-09-22 |
| Reported by FDA | 2018-10-03 |
| Terminated | 2020-05-26 |
| Distributed | Nationwide (US) |
| Quantity | 233 |
| Reason classes | software |
| Model numbers | 983031 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3240-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.