Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22544 |
| Brand Name: | AQUIOS CL Flow Cytometry System |
| Model: | |
| Affected: | All software |
| 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 identified that the AQUIOS CL Flow Cytometer may process the same sample with two different sample IDs and sample information while using the single tube loader. This issue has the potential for erroneous results due to the mis-identification. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/1/2018 |
