Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Canon Full Auto Ref-Keratometer RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received 17 claims from our...
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 Canon Inc. directly.
Affected Products
Canon Full Auto Ref-Keratometer RK-F2, Catalog Number 6937B002AA. Product Usage: This device is intended to be used to measure the refractive power and the radius of corneal curvature of the human eye.
Quantity: 384 units
Why Was This Recalled?
Canon Inc. had received 17 claims from our foreign sales companies between October to November 2012 that measurement value of RK-F2s refractive power (SPH value) sometimes indicated abnormal value which occurs approximately 5% in probability.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Canon Inc.
Canon Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report