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Previous Investigations Other Litigations ReNu MoistureLoc Research Center

Litigation Proliferates, 10.07

in this section: FDA ReNu Recall | FDA: Failure to Report, 11.06 | B&L Responds: ReNu FDA Letter 11.06 | FDA Warning | Litigation Proliferates, 10.07 | FDA Supports Withdrawal | FDA Public Health Notice | B&L Sales Fall | Bausch & Lomb Press Release | MultiPlus Recall, 3/07 | ReNu lawsuit


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Breaking News on ReNu Contact Lens Solution Litigation: 573 Lawsuits

Weitz & Luxenberg is no longer accepting ReNu with MoistureLoc cases.

October 29, 2007--BREAKING NEWS ON RENU LITIGATION: Makers of ReNu With MoistureLoc, Bausch & Lomb, Inc., has been slapped with 573 product liability lawsuits related to the defective contact lens solution, according to the Rochester Business Journal.

Of 344 ReNu claims filed in state courts, 308 cases have been consolidated in Supreme Court in New York City.

Last year, the Food and Drug Administration sent a warning letter to Bausch & Lomb for its "failure to establish and maintain procedures for the control of storage areas and stock rooms for product to prevent mix-ups, damage, deterioration, contamination, or other adverse effects" related to its production of ReNu solution in its Greenville, SC facility.

On August, 23, 2006, a US research report revealed that one-third of patients with a serious eye infection associated with the ReNu with MoistureLoc product had such severe infections that they had or will need a corneal transplant. Weitz & Luxenberg has spearheaded litigation related to the dangerous contact-lens solution, filing its first of several corneal transplant cases with the State Supreme Court of New York on May 5, 2006, court index # 106201/06.

If you have developed an severe eye infection resulting in vision loss after using ReNu contact lens solution, you may have a lawsuit claim against the manufacturer, Bausch & Lomb. To inquire about your possible ReNu lawsuit, fill out the form below for a free case evaluation. We will be in touch shortly.



see also:

MultiPlus Recall, 3/07 FDA Alert: Bausch & Lomb Recall of 12 Lots of ReNu MultiPlus Solution
Customers cite discolored multiplus solution; B&L issues recall

B&L Responds: ReNu FDA Letter 11.06 Bausch & Lomb Responds to FDA Warning Letter on ReNu
B&L Response to FDA on failure to disclose ReNu foreign fungal cases

News & Warnings ReNu Lawsuit - Bausch & Lomb’s Contact Lens Solution News & Warnings
Keep up to date with ReNu Brand contact lens solution News & Warnings

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