Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 18609 |
| Brand Name: | Maquet Magnus Hybrid OR Table |
| Model: | 1180.01B2 |
| Affected: | Serial numbers: 00001 to 00100 |
| Software version: | |
| Recalling Organisation: | Maquet Australia Pty Ltd (NZ) 12G Andromeda Cres East Tamaki Auckland 2013 |
| Contact Information: | 021 874 882 |
| Manufacturer: | Maquet GmbH |
| Issue: | Report of a collision between the C-arm of the angiography-system and the MAGNUS OR table system. The root cause analysis has shown that the MAGNUS column provided wrong position data of the longitudinal movement. Thus the collision calculation of the angiography-system led to a wrong result. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/6/2015 |
