Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25036 |
| Brand Name: | Medifab Shuttle Discovery System ( Pushchair and Indoor base options with seating system) |
| Model: | Verve Stroller |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Medifab Limited 1 Pereita Drive Rolleston 7675 |
| Contact Information: | 0800 543 343 |
| Manufacturer: | Medifab Limited |
| Issue: | The manufacturer has identified that if the antivibration nut is overtightened, it will damage the T bolt within the folding joint which will lead to a greater gap at the folding joint. This could provide a finger entrapment for the user and anyone interacting with the frame, potentially leading to serious injury. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/9/2019 |
