Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are Recalled by Rayner Intraocular Lenses Limited Due to Firm become aware of reports of post-operative refractive...
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 Rayner Intraocular Lenses Limited directly.
Affected Products
C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the capsular bag of the human eye as a replacement for the crystalline lens following phacoemulsification
Quantity: 49
Why Was This Recalled?
Firm become aware of reports of post-operative refractive errors following implantation of lenses.
Where Was This Sold?
This product was distributed to 1 state: MO
About Rayner Intraocular Lenses Limited
Rayner Intraocular Lenses Limited 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