Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21126 |
| Brand Name: | Olympus OER-AW Endoscope Reprocessor |
| Model: | |
| Affected: | Updated Version of Operation Manual: Relevant for models: JF-20, JF-140F, TJF-M20, TJF-30, TJF-145, TJF-140F, TJF-150, TJF-160F, TJF-160VF and TJF-Q180V. |
| Software version: | |
| Recalling Organisation: | Olympus (NZ) Ltd 15D Paul Matthews Road Albany Auckland |
| Contact Information: | 0508 659 6787 |
| Manufacturer: | Olympus Medical Systems Corporation |
| Issue: | The Operation Manual for the OER-AW Endoscope Reprocessor has been updated to instruct users of non-detachable distal cover type duodenoscopes, such as the TJF-Q180V duodenoscope, to follow the precleaning and manual cleaning as stated in the duodenoscope's reprocessing manual prior to setting them into the OER-AW. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/2/2017 |
