FDA recall record

Novartis Consumer Health Theraflu recall — FDA D-751-2014

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

Class IIclassification
D-751-2014official record ID
Jan 29, 2014report date

Recall record at a glance

Official recordD-751-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNovartis Consumer Health
Report dateJan 29, 2014
Recall initiation dateJun 18, 2013
Quantity1,140,564 cartons
LocationLincoln, NE, United States

Official product description

Theraflu (acetaminophen 325 mg, pheniramine maleate 20 mg, phenylephrine hydrochloride 10 mg) powder packets, Natural Lemon flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, labeled as a) Theraflu Sinus & Cold (NDC 0067-6319-06, UPC 3 0043-6319-06 7) and b) Theraflu Cold & Sore Throat (NDC 0067-6716-06, UPC 3 0043-0467-16 0). Also packaged under foreign labels: NeoCitran Cold & Flu powder packets, Natural Source Lemon flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, UPC 0 58478 05009 6; and Theraflu Exthegran powder packets, lemon flavor, packaged in a) 6-count packets per carton (UPC 7 501124 812904) and b) 10-count packets per carton (UPC 7 501124 814588), Distributed by Novartis Farmaceutica S.A. De C.V., Mexico

Why the product was recalled

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

Distribution information

Nationwide, Mexico, Russia, Korea, Panama, China, and Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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