US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 7, 2017 (10 years ago)

Montelukast sodium tablets, 10 mg, 30-count bottle, Rx Only, Manufactured for: Camber…

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

Why it was recalled

Discoloration: the firm received a complaint of a sealed bottle in which tablets inside had blue spots and a blue powder inside the bottle.

What was recalled

Montelukast sodium tablets, 10 mg, 30-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: HETERO Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-726-30

Recalling firm
Hetero USA Inc
NDC code
31722-726-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0623-2017

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.

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