Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29575 |
| Brand Name: | Stryker JR (HOC) - 2a - Knee tibia trial prosthesis |
| Model: | 5530-T-209Y (TRIATHLON SOLID CR TIBIAL INSERT TRIAL SIZE 2 - 9MM), 5530-T-210Y (TRIATHLON SOLID CR TIBIAL INSERT TRIAL SIZE 2 - 10MM) |
| Affected: | A234P, A234Q |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Howmedica Osteonics Corp |
| Issue: | The manufacturer has discovered that certain lots of the Triathlon Solid CR Tibial Insert Trials may contain product with incorrect thickness laser marking. The scope of this issue is limited to Catalog Number 5530-T-209Y, Lot A234P and Catalog Number 5530-T-210Y, Lot A234Q. These catalog numbers are found in the tray, 5530T27Y-T. This is the TRIATHLON® CR INSERT TRIAL tray. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/6/2022 |
