US Drug Recall Register
Class III · Low risk Terminated Initiated May 15, 2013 (13 years ago)

Maximum Strength Comtrex ,Severe Cold & Sinus Acetaminophen 325mg, Chlorpheniramine…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.

What was recalled

Maximum Strength Comtrex ,Severe Cold & Sinus Acetaminophen 325mg, Chlorpheniramine Maleate 2mg, Phenylephrine HCL 5mg, packaged in 12 coated caplets daytime formula and 12 coated caplets nighttime formula. Novartis, distributed by: Novartis Consumer Health, Inc., Parsippany, NJ. 07054-0622, NDC 0067-2081-24

Recalling firm
Novartis Consumer Health
NDC code
0067-2081-24
Origin
NE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-741-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Phenylephrine recalls

See all