US Drug Recall Register
Class I · High risk Terminated Initiated Jan 3, 2013 (14 years ago)

Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.

What was recalled

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.

Recalling firm
Mobius Therapeutics LLC
NDC code
49771-002-01
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-809-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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