Bausch & Lomb Surgical, Inc.: Medical Device Recalls in 2015

According to to data from the FDA, there were 2 medical device recalls made by Bausch & Lomb Surgical, Inc. in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

• Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: The SofPort/SoFlex IOLs are intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.
• Bausch & Lomb SofPort Advanced Optics Aspheric Lens