Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22097 |
| Brand Name: | AQUIOS CL Flow Cytometry System |
| Model: | |
| Affected: | software versions (2.0, 2.0.1 and 2.1) |
| 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 Inc |
| Issue: | The manufacturer is advising that when AQUIOS CL systems are connected to a Laboratory Information System (LIS), the system may duplicate sample requests leading to sample mis-identification. This is an updated notification in follow-up to the previous communication received (dated 16 October 2017) concerning duplicate sample requests leading to sample mis-identification when using the AQUIOS CL systems connected to a Laboratory Information System (LIS). This important information needs immediate attention. The information replaces the instructions in the original notification dated 16 October 2017. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/12/2017 |
