Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20442 |
| Brand Name: | ASP Sterrad100NX System |
| Model: | |
| Affected: | Part numbers 10104, 10104002, 10104003 and 10104004 |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (New Zealand) Limited 507 Mt Wellington Highway Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | Advanced Sterilization Products Inc |
| Issue: | The STERRAD® 100NX® systems require a CTick label (RCM) be applied to comply with the Ministry of Business, Innovation and Employment, Radiocommunications (Compliance) Notice 2013 No. 2.. This labelling will be performed by a Johnson & Johnson Pty Ltd (JJM) representative. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/7/2016 |
