Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20571 |
| Brand Name: | Stryker Surgical procedure kit, orthopaedic, reusable - Mahwah (reamers) |
| Model: | |
| Affected: | Trident Universal Impactor/Positioner( P/N: 2101-0200) |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Howmedica Osteonics |
| Issue: | Upon investigation, it was determined that the press fit between the threaded stud and the handle shaft assembly for the Trident Universal Impactor/Positioner (P/N: 2101-0200) may lead to the gradual protrusion of the threaded stud over time. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/8/2016 |
