Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STAAR AQ Cartridge-FP Recalled by Staar Surgical Co. Due to The STAAR AQ Cartridge-FP may malfunction and may...
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 Staar Surgical Co. directly.
Affected Products
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Quantity: 2,612 units
Why Was This Recalled?
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
Where Was This Sold?
US
About Staar Surgical Co.
Staar Surgical Co. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report