Reported Apr 29, 2015 · Terminated
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch…
Reckitt Benckiser LLC
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Reckitt Benckiser LLC · 399 Interpace Pkwy · Parsippany, NJ · 07054-1133
Is this the product you have?
- Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England
- Lot codes and dates
Lot BD375 exp 06/2016BD566BD661 exp. 08/2016
- Amount recalled
- 155 cases (2000 pouches of 2 tablets per case)
Where it was sold
- Nationwide
Why it was recalled
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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