Product Wiki · Recalls · Health Canada — Medical Devices

SPECTRALIS® with Flex Module — recall 82505

Health Canada — Medical Devices · Canada · 2026-08-19 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
82505
Date of alert
2026-08-19
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Ophthalmology
Product type
Medical devices
Reported risk: There is a possibility that the castor wheels of the Flex stand are not properly attached. The wheels may come loose. As a result, the Flex stand may tip over. Users shall schedule a service appointment as soon as possible so that the castor fastenings can be inspected and corrected.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/spectralisr-flex-module

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