Bausch & Lomb Inc Contact lens solution. The product is distributed under the following trade names: Bausch & Lomb ReNu Multi-Plus Multi-Purpose Solution, Equate Multi-Purpose Solution and Target Brand Multi-Purpose Solution. The product is distributed in up to three sizes: 4 fl.oz., 12 fl. oz. and 16 fl. oz Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Contact lens solution. The product is distributed under the following trade names: Bausch & Lomb ReNu Multi-Plus Multi-Purpose Solution, Equate Multi-Purpose Solution and Target Brand Multi-Purpose Solution. The product is distributed in up to three sizes: 4 fl.oz., 12 fl. oz. and 16 fl. oz
Brand
Bausch & Lomb Inc
Lot Codes / Batch Numbers
Lot numbers appearing on the bottles distributed in the U.S.: GC6030, GC6037, GC6045, GC6061, GC6063, GC6072, GC6048 and GC6052.
Products Sold
Lot numbers appearing on the bottles distributed in the U.S.: GC6030, GC6037, GC6045, GC6061, GC6063, GC6072, GC6073 and GC6085. The lots all carry the expiration date ''2008-03'' on the bottle. Lot numbers appearing on bottles distributed only outside of the U.S.: GC6038, GC6048 and GC6052.
Bausch & Lomb Inc is recalling Contact lens solution. The product is distributed under the following trade names: Bausch & Lomb Re due to A higher than expected amount of trace iron in some bottles of finished product that over time affects the product's stability and color.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A higher than expected amount of trace iron in some bottles of finished product that over time affects the product's stability and color.
Recommended Action
Per FDA guidance
The firm issued a press release on 03/05/2006. Consignees were notified on 03/06/2007 via a customized Recall Notification Package via overnight courier with tracking and delivery confirmation capability. Bausch & Lomb Sales Representatives will visit the home offices of the major wholesale and distributors concurrent with the mailing of the notification packages.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026