Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: Recalled by Carl Zeiss Meditec AG Due to Due to the incorrect DC/DC converter being assembled...
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
Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values and keratometric characteristics of the human eye. The results are used to assist the process of prescribing optical aids such as eyeglasses and contact lenses.
Quantity: 132 units
Why Was This Recalled?
Due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety function of the board would be insufficient resulting in an increased leakage of current and potentially cause electrical shocks to the user.
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