Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23443 |
| Brand Name: | Stryker GmbH - Fixation device, external, system |
| Model: | |
| Affected: | 983031 Hoffmann LRF Hexapod Software HLRF 1.1-2/002 and 983031 Hoffmann LRF Hexapod Software HLRF 1.0-2/002 |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker GmbH |
| Issue: | The manufacturer has identified a deviation with the Hoffmann LRF Hexapod Software that occurs when both the Correct Axial First feature is selected and more than one correction per day is selected when computing a correction plan. The deviation results in the calculation of an accelerated correction plan for the axial portion of the plan. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/8/2018 |
