Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21430 |
| Brand Name: | X-ray system, fluoroscopic, general-purpose, mobile, digital |
| Model: | |
| Affected: | OEC Elite Device Labeling Issue |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | OEC Medical Systems Inc |
| Issue: | The manufacturer recently identified that product use labels on certain OEC Elite systems were missing or applied in the incorrect location on the device. The missing labels have the potential to result in users overlooking safe operating practices and exposing themselves or others to potential hazards that may lead to significant harm. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/5/2017 |
