Recalled Mitosol products may be identified by:
- expiration date: August 2013
- lot numbers: M098260 and M086920
- distribution dates: October 22, 2012- December 14, 2012
What to Do with Recalled Mitosol
Mobius has informed consumers of the recall via email, telephone and mail. Officials advise anyone who possesses recalled Mitosol products to call Mobius at 1-877-393-6486 for information on how to return the product and to schedule a replacement from unaffected lots. The U.S. Food and Drug Administration urges physicians and customers not to use any recalled products. Treatments performed with recalled Mitosol can result in:
- severe eye damage
- eye infections
- vision loss or blindness
If you suffer from any serious side effects associated with the use of recalled Mitosol, contact the FDA MedWatch Adverse Event Reporting Program. FDA assistance may be found by:
- faxing 1-800-FDA-0178
- visiting www.fda.gov/medwatch/report.htm
- mailing the FDA a pre-addressed form found online here
For legal assistance through our expert attorneys, fill out the “Request Attorney Assistance” form located in the upper-right section of this page.