Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24067 |
| Brand Name: | EQUIA Forte Fil, GC Fuji VII Capsule, GC Fuji VIIEP Capsule, GC Fuji VIII, GF, GC Fuji Bulk, GP Capsule, Fuji I, Fuji I Capsule, Fuji II Capsule, Fuji II LC Capsule, II LC Improved, Fuji IX EXTRA, GC Fuji IX GP, IX GP Fast Capsule, Fuji ORTHO Band, GC Fuj |
| Model: | |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Henry Schein Regional Ltd 243-249 Bush Road Rosedale North Shore City Auckland 0632 |
| Contact Information: | 0800 808 855 |
| Manufacturer: | GC Europe NV |
| Issue: | The manufacturer has identified an issue with a defective dental cement applicator system. When preparing the cement following the IFU, there have been reports of the cement either paritally extruding, or not extruding. The dentest is expected to identify the faulty unit before application to the patient. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/1/2019 |
