Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.
Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Mobius Therapeutics LLC to request your refund or repair — edit it as you like.
Subject: Recall D-809-2013 — Mobius Therapeutics LLC Mobius Therapeutics LLC recalls Mitosol (mitomycin for solution), 0.2 mg/via Hello, I own a 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 that is covered by recall D-809-2013 from Mobius Therapeutics LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.