Mobius Therapeutics LLC recalls Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC 49771-002-
Recalled July 31, 2013 · FDA recall D-809-2013 · Mobius Therapeutics
Hazard
Non-Sterility: one or more components of the kit have been found to be contaminated with yeast. · FDA Class I
Units
83 boxes
Sold at
Nationwide and Military and Government Consignees
Description
Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.
Product
Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC 49771-002-03), Rx only, Manufactured for: Mobius Therapeutics, LLC, 4041 Forest Park Avenue, St. Louis, MO 63108 USA.
Manufacturer(s)
Mobius Therapeutics LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →