Mucinex DM recall
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
Why was Mucinex DM recalled?
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot BD375 exp 06/2016; BD566, BD661 exp. 08/2016
- Product
- 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
- Recalling firm
- Reckitt Benckiser LLC
- Quantity
- 155 cases (2000 pouches of 2 tablets per case)
- Distribution
- Nationwide
- Recall date
- April 29, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)