We have received a product recall request from Bausch and Lomb for Renu solutions. Bausch and Lomb have assured us that there is very low risk to anyone that has used these products and they are voluntarily recalling these products as a precaution (further information at the end of this notice).
This only affects a handful of products with specific lot and batch numbers. We are contacting all patients directly that use this product and asking them to check any that they still have. The products effected are both the larger regular supply bottles that come in a box of 3 and also the smaller trial/travel sized bottles you may have collected from the practice.
If you do have some please refrain from using anymore and get in touch with us.
The lot numbers recalled are below and can be found on each of the products
Information from B&L website
This voluntary recall follows a notification received by Bausch + Lomb from one of its third-party suppliers in Milan, Italy, which sterilizes some components (bottles, plugs and caps) of these products prior to manufacturing in our facility in Milan, Italy, of a compliance issue with its sterilization process. Bausch + Lomb is one of many companies impacted by this situation.
The health and safety of everyone who uses our products is our utmost priority. While there is a low risk of infection with these products, Bausch + Lomb has chosen to voluntarily recall these certain lots of products because we cannot confirm the supplier’s conformance to process compliance requirements for some of the components of these products. No serious adverse events have been reported to date in association with this issue.
For full details from B&L please visit