FDAOctober 12, 2016device

Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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Further investigation found that repackaged Algerbrush-II and its accessories from April 30, 2012 to present, contained out of date operating instruction.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.

What to do

FDA enforcement status: Terminated

Brands named

bausch lombbauschbausch lomb

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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