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Novartis Consumer Health recalls Theraflu Multi-Symptom Severe Cold (acetaminophen 500 mg, dextromethorphan hydrobromide 20 mg, phenylephrine hydrochlori

Recalled January 29, 2014 · FDA recall D-752-2014 · Novartis Consumer Health

Hazard
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances. · FDA Class II
Units
1,202,960 cartons and cards
Sold at
Nationwide, Mexico, Russia, Korea, Panama, China, and Canada.

Description

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Product
Theraflu Multi-Symptom Severe Cold (acetaminophen 500 mg, dextromethorphan hydrobromide 20 mg, phenylephrine hydrochloride 10 mg) powder packets, Green Tea & Honey Lemon flavors, packaged in a) 6-count packets per carton (NDC 0067-6426-06, UPC 3 0067-6426-06 8) and b) 1-count packet per card (NDC 0067-6426-01, UPC 3 0067-6426-01 3), Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622.
Manufacturer(s)
Novartis Consumer Health

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Novartis Consumer Health recalls Theraflu Multi-Symptom Severe Cold (acetaminophen 500 mg, dextromethorphan hydrobromide 20 mg, phenylephrine hydrochlori | RecallWatchUSA