Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints database was reviewed and there have...
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 Bausch & Lomb Inc Irb directly.
Affected Products
LASEREDGE Knives, CRESCENT BLADE STRAIGHT BEVEL UP STR (6/BOX), REF/PRODUCT CODE E7500, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
Quantity: 1,236,749 knives in total
Why Was This Recalled?
The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bausch & Lomb Inc Irb
Bausch & Lomb Inc Irb has 48 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report