Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product 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 VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of contact lenses and spectacle lenses and displaying measurement values for sphere, cylinder and prism.
Quantity: 603 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