Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14161 |
| Brand Name: | Fujifilm FCR Go2 Mobile X-Ray System |
| Model: | Model: FCR-MB 201 |
| Affected: | APL software versions below V1.21 |
| Software version: | |
| Recalling Organisation: | Fujifilm NZ Limited 2c William Pickering Drive Albany Auckland |
| Contact Information: | 0800 242 646 |
| Manufacturer: | Fujifilm Corporation |
| Issue: | It has been confirmed that in rare cases the exposure conditions to the values initially entered from Console are reset when turning on the collimator lamp while pressing the collimator hand switch (releasing the electromagnetic brake) where the exposure conditions (kV and mAs values) entered from Console are changed manually on the control panel of the unit. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/2/2013 |
