Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28138 |
| Brand Name: | DxA 5000 |
| Model: | DxA System |
| Affected: | |
| 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 has received reports of sample carriers (with or without samples) getting routed to the outer lane of the Single Drive Transport Segment (B57634) to the end of the lane, then dropped off the lane. The outer lane is not intended to route tubes per DxA system design specification, therefore there is no physical barrier at the end to physically restrain sample carriers. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/8/2021 |
