Failed Impurities/Degradation Specifications: High out of specification results for the known impurity p-Aminophenol.
Failed Impurities/Degradation Specifications: High out of specification results for the known impurity p-Aminophenol.
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 Qualitest Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0331-2015 — Qualitest Pharmaceuticals Qualitest Pharmaceuticals recalls ACETAMINOPHEN and CODEINE PHOSPHATE ORA Hello, I own a Qualitest Pharmaceuticals recalls ACETAMINOPHEN and CODEINE PHOSPHATE ORAL SOLUTION USP, 120 mg/12 mg per 5 mL, packaged in a) 4 oz. (120 mL) bottles, that is covered by recall D-0331-2015 from Qualitest Pharmaceuticals. 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.
