| Type of Product |
Medical Device |
| TGA Recall Reference |
RC-2016-RN-00996-1 |
| Product Name/Description |
Sterrad 100NX system (Sterilisation system)
Part Numbers: 10104, 10104002, 10104003, 10104004
ARTG Number: 123603 |
| Recall Action Level |
Hospital |
| Recall Action Classification |
Class III |
| Recall Action Commencement Date |
26/07/2016 |
| Responsible Entity |
|
| Reason/Issue |
Johnson & Johnson Medical (JJM) is advising that the Sterrad 100NX system requires a CTick label (RFID) be applied to comply with the Australian Communications and Media Authority (ACMA) spectrum licensing and CTick requirements. |
| Recall Action |
Recall for Product Correction |
| Recall Action Instructions |
Johnson & Johnson Medical will be attending all sites to place the required label on the affected devices. This action has been closed-out on 13/07/2017. |
| Contact Information |
02 9815 3765 - Johnson & Johnson Medical |