Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28743 |
| Brand Name: | AU/DxC AU Magnesium |
| Model: | OSR6189 |
| Affected: | DxC AU Magnesium |
| Software version: | |
| Recalling Organisation: | Beckman Coulter NZ Ltd Suite 2, Level 4 30 St Benedicts Street Newton AUCKLAND |
| Contact Information: | 0800 446 109 |
| Manufacturer: | Beckman Coulter Ireland Inc |
| Issue: | The manufacturer has determined that the Magnesium failed to meet the lipemic interference specification for the serum application as defined in the IFU: Interference less than 10% up to 500 mg/dL Intralipid. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/12/2021 |
