Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by Bausch & Lomb, Inc. Due to According to firm ( Bausch & Lomb, Inc....
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. directly.
Affected Products
Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient
Quantity: 2487 units Domestic (USA), 1,211 units Foreign (outside USA)
Why Was This Recalled?
According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging operator notified his supervisor he had not placed the operating instruction into the last repackaging of SKU 0816 C (Pterygium Burr Medium Diamond). Further investigation found that repackaged Algerbrush-II and its accessories from April 30, 2012 to present, contained out of date operating instruction. Therefore Bausch & Lomb is proposing a Field Correction to provide customer purchasing product from April 30, 2012 to June 20, 2016 with the current operating instruction.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bausch & Lomb, Inc.
Bausch & Lomb, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report