Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec AG Due to IOL Master software versions 7.5 and 7.7 calculation...
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
IOL Master 5.5: Software versions 7.5 and 7.7; Ophthalmic: used to obtain ocular measurements and perform calculations to allow physicians to determine appropriate IOL power and type for implantation.
Quantity: 49
Why Was This Recalled?
IOL Master software versions 7.5 and 7.7 calculation printouts and exported reports can contain the wrong IOL power 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