Data Foundry

Drug recalls 2014

Theraflu MAX-D Severe Cold & Flu — Class II drug recall D-753-2014

Terminated recall by Novartis Consumer Health, reported 2014-01-29, distributed nationwide. Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Recall numberD-753-2014
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNovartis Consumer Health, Lincoln, NE, United States
Recall initiated2013-06-18
Classified2014-01-17
Reported by FDA2014-01-29
Terminated2014-11-04
DistributedNationwide (US)
Countries outside the USCA, CN, KR, MX, PA, RU
Quantity868,104 cartons
UPC / GTIN / UDI-DI00058478107011
NDC00067-6427-06
Lot numbers10089568, 10093324, 10094745, 10097626, 10097627, 10098588
Expiration dates2013-05-31, 2013-07-31, 2013-09-30, 2013-10-31, 2013-11-30, 2014-01-31, 2014-06-30, 2014-09-30

Product

Theraflu MAX-D Severe Cold & Flu (acetaminophen 1000 mg, dextromethorphan HBr 30 mg, guaifenesin 400 mg, pseudoephedrine HCl 60 mg) powder packets, Natural Citrus flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, NDC 0067-6427-06, UPC 3 0067-6427-06 5. Also packaged under foreign label: NeoCitran Extra Strength Total 7 Symptom Relief Plus Mucous Relief powder packets, Soothing Lemon flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, UPC 0 58478 10701 1.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-753-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.