Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20292 |
| Brand Name: | Stryker TRident Constrained Liner Impactor Tips |
| Model: | 21992022, 21992028 and 21992032 |
| Affected: | All lots affected |
| 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: | During steam sterilisation validation the Trident Constrained Liner Impactor Tips do not meet the required Sterility Assurance Level (SAL) of 10-6. These instruments are sterilised at the hospital prior to surgery and are not distributed as sterile. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/6/2016 |
