Reported Jul 31, 2013 · Terminated

Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC…

Mobius Therapeutics LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mobius Therapeutics LLC · 4041 Forest Park Ave · Saint Louis, MO · 63108-3213

Is this the product you have?

    • 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 forMobius Therapeutics, LLC, 4041 Forest Park Avenue, St. Louis, MO 63108 USA
Lot codes and dates
    • Lot #: M086920 and M098260
    • Exp. 08/2013
Amount recalled
83 boxes

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

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

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 29, 2013 · Data as of Sep 19, 6:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.