Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24603 |
| Brand Name: | RIFTON TRAM & E-Pacer units |
| Model: | |
| Affected: | K310 and K320 TRAMs manufactured between July 4, 2012 and April 4, 2018; K660 E-Pacers manufactured between June 12, 2017 and April 5, 2018. |
| Software version: | |
| Recalling Organisation: | Medix 21 Ltd 7 Mana Esplanade Paremata Porirua |
| Contact Information: | 04 233 1627 |
| Manufacturer: | Rifton Equipment |
| Issue: | The manufacturer has received complaints of buckles failing to latch securely, presenting a risk of falling. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Public Recall |
| Date Commenced: | 23/5/2019 |
