Failed Impurities/Degradation Specifications: Presence of an impurity peak that exceeds approved specification.
Failed Impurities/Degradation Specifications: Presence of an impurity peak that exceeds approved specification.
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 VistaPharm, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0869-2017 — VistaPharm, Inc. VistaPharm, Inc. recalls Nystatin Oral Suspension, USP, 100,000 units/mL, packaged Hello, I own a VistaPharm, Inc. recalls Nystatin Oral Suspension, USP, 100,000 units/mL, packaged in a) 2 fl.oz. (60mL) bottles (NDC 66689-008-02), and 500,000 that is covered by recall D-0869-2017 from VistaPharm, Inc.. 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.
