Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22556 |
| Brand Name: | Lights - Ardon |
| Model: | |
| Affected: | Spring arm part number, ARD567910974, ARD568301798, ARD568301799 |
| Software version: | |
| Recalling Organisation: | Getinge Australia Pty Ltd (NZ) Unit D, Ground Floor, Building A, Millenium Centre 600 Great South Rd Ellerslie Auckland 1051 |
| Contact Information: | 09 272 9039 |
| Manufacturer: | Maquet SA |
| Issue: | The manufacturer has received complaints concerning unintentional drifting of the cupola during surgery due to prematurely worn out brake screws. The observed movement is a slow rotation of the cupola around the axis, potentially shifting the light patch away from the wound. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/2/2018 |
