FDA Drug Recalls

Recalls / Class II

Class IID-760-2014

Product

NeoCitran DM Cough & Cold (dextromethorphan hydrobromide 30 mg, phenylephrine hydrochloride 10 mg, pheniramine maleate 20 mg) powder packets, Natural Source Lemon flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, UPC 0 58478 05503 9.

Affected lot / code info
Lot #: 10122293, Exp 8/31/2013.

Why it was recalled

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

Recalling firm

Firm
Novartis Consumer Health
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
10401 Hwy 6, Lincoln, Nebraska 68517-9626

Distribution

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

Timeline

Recall initiated
2013-06-18
FDA classified
2014-01-17
Posted by FDA
2014-01-29
Terminated
2014-11-04
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-760-2014. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls