Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22031 |
| Brand Name: | Medtronic O-arm O2 Surgical Imaging System |
| Model: | |
| Affected: | model number BI-700-02000 |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Navigation Inc |
| Issue: | During servicing of certain internal components of the O-armTM O2, it was identified that the high-power cable connector may come in contact with surrounding metal (toggle switch or corner of battery tray) during the disconnecting/reconnecting process. If this occurs it could result in an electrical short and a shock to the field service technician.The manufacturer will be installing a service kit on the O-armTM O2 surgical imaging system to further enhance the safety of field service personnel. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/9/2017 |
