RecallRadar

FDA Drug recall D-758-2014

NeoCitran (acetaminophen 1000 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 30 mg, chlorpheniramine maleate 4 mg)…

On 2014-01-29 the FDA classified a Class II recall of NeoCitran (acetaminophen 1000 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 30 mg, chlorpheniramine maleate 4 mg)… by Novartis Consumer Health, citing presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-758-2014
ClassificationClass II
Statusterminated
Initiated2013-06-18
Published2014-01-29
Last updated2026-09-13 11:51 UTC
CompanyNovartis Consumer Health
DistributionUS

Product

NeoCitran (acetaminophen 1000 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 30 mg, chlorpheniramine maleate 4 mg) powder packets, Natural Source Cherry flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, labeled as a) NeoCitran Ultra Strength Total Flu 7 Symptom Relief (UPC 0 58478 47365 9) and b) NeoCitran Extra Strength Sore Throat & Cough (UPC 0 58478 47365 9).

Reason

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

Identifiers

upc058478473659
code_infoLot #: a) 10112236, Exp 4/30/2014 and 10122295, Exp 9/30/2014; b) 10093319, Exp 6/30/2013 and 10100417, Exp 9/30/2013.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-758-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.