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Bausch + Lomb Voluntarily Recall Three Lots of R

Bausch + Lomb Voluntarily Recall Three Lots of ReNu® Multi-Purpose Solution

December 2010

Bausch + Lomb is conducting a voluntary recall of three lots (C9116, C9009, C9048) of their ReNu® Multi-Purpose Solution in Europe, Guadeloupe, Martinique and Réunion

Routine testing has shown that these lots may not meet all specification criteria at the end-of-shelf life
No other Bausch + Lomb products, including other lots of ReNu® Multi-Purpose solutions are affected by this voluntary recall. 

Bausch + Lomb decided to initiate the quality-related recall after their Stability Monitoring Program showed that the performance trend of certain lots did not meet their expectations. There is no indication of a safety or efficacy issue and there have been no reported adverse events. This recall is being conducted as a precaution.

B & L have contacted retailers and eye care professionals who have been shipped this product to initiate the recall and inform them of the steps they should take to return  the product to them. However, due to the time elapsed since production they do not anticipate that there is any stock remaining.

 
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