Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software defect in the FORUM Viewer versions 3.1...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Carl Zeiss Meditec AG directly.
Affected Products
FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1) 000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1); 000000-2084-928 (USB drive with FORUM 3.2.1) Ophthalmic image management system.
Quantity: 985
Why Was This Recalled?
Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to misinterpretation of the optical coherence tomography (OCT) data.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carl Zeiss Meditec AG
Carl Zeiss Meditec AG has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report