Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29769 |
| Brand Name: | Automated Endoscope Reprocessor |
| Model: | Getinge ED-Flow AER (Automated Endoscope Reprocessor); and Getinge ED-Flow SD AER - multiple serial numbers |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Getinge Australia Pty Ltd (NZ) Unit D, Ground Floor, Building A, Millenium Centre 600 Great South Rd Ellerslie Auckland 1051 |
| Contact Information: | 09 272 9039 |
| Manufacturer: | Getinge Lancer |
| Issue: | The manufacturer has discovered that a temperature sensor in the ED-FLOW AER chamber may not work as intended and may provide incorrect temperature readings for washing and disinfection temperature during process. The result on the process ticket has shown OK despite the temperature not having reached the parameters required for validated biocidal activity. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/8/2022 |
