Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25393 |
| Brand Name: | Afterloader |
| Model: | Sites affected will be - Flexitron HDR/PDR and Flexitron Co-60 systems |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Elekta Pty Limited - New Zealand Branch Suite 302, Geyser Building, 100 Parnell Road Parnell AUCKLAND 1052 |
| Contact Information: | 0273-544-793 |
| Manufacturer: | Nucletron BV |
| Issue: | In case of a component failure of the Flexitron internal check cable or source cable guide mechanism, a treatment interruption or incorrect source positioning can occur. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/11/2019 |
