Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27005 |
| Brand Name: | IOLMaster |
| Model: | ZEISS IOLMaster 700 |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Carl Zeiss (NZ) Ltd 22 Fremlin Place Avondale Auckland 1026 |
| Contact Information: | 09 838 5626 |
| Manufacturer: | Carl Zeiss Meditec AG |
| Issue: | The manufacturer has indentified that the ZEISS IOLMaster 700 with software version 1.90.2.09 and 1.90.8.06, when used in conjunction with modality worklist (MWL) functionality, is not per-forming as expected. In rare cases this leads to a false display of patients in the patient manager screen, which can subsequently lead to the implantation of an incorrect intraocular lens (IOL). |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/12/2020 |
