Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to Possible dull knife edge
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 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Quantity: 384 packs/6 blades (2,304 individual blades)
Why Was This Recalled?
Possible dull knife edge
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