Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19552 |
| Brand Name: | Synthes Kirschner Wire |
| Model: | Part No: 02.113.001 |
| Affected: | All Lot numbers |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (NZ) Limited 13a Gabador Place Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | Synthes GmbH |
| Issue: | The Kirschner wire is made from Co35Ni35Cr20Mo10 (MP35N) which is cobalt based alloy containing 35% nickel. However, the label and technique guide incorrectly indicate that the devices are made of stainless steel. The product is shipped with an insert which references the potential risk of allergy/hypersensitivity reactions, but there is no specific information on the label or in the technique guide with regards to the percentage of nickel content in the devices. Please note: - Product shipped in "kits" in New Zealand are not in packaging and therefore not labelled |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/12/2015 |
