Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
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 Reckitt Benckiser LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0964-2015 — Reckitt Benckiser LLC Reckitt Benckiser LLC recalls Mucinex DM (guaifenesin 600mg and dextromethorp Hello, I own a Reckitt Benckiser LLC recalls Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch that is covered by recall D-0964-2015 from Reckitt Benckiser 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.
