Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination data and patient name may be mixed...
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 Haag-Streit USA Inc directly.
Affected Products
Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
Why Was This Recalled?
Examination data and patient name may be mixed up when printing or generating a pdf with the interface at Pacific Coast and Laser Institute (PCLI).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Haag-Streit USA Inc
Haag-Streit USA Inc has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report