Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20815 |
| Brand Name: | Stryker Trauma Fixation device, internal T2 K wire |
| Model: | |
| Affected: | 12106450S - GAM Kirschner Wire, 18060050S - T2 K-Wire, 18063030S - T2 K-Wire Recon |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Trauma AG |
| Issue: | It was found through review of packaging that the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a manufacturing error. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/11/2016 |
