US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 20, 2018 (8 years ago)

Montelukast Sodium Tablets, 10 mg*, 30-count bottles, Rx Only, By: Hetero, Hetero Labs…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Discoloration: A complaint was received from a pharmacist for the presence of blue specks on tablets.

What was recalled

Montelukast Sodium Tablets, 10 mg*, 30-count bottles, Rx Only, By: Hetero, Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, NDC 31722-726-30.

Recalling firm
Hetero Labs Limited Unit V
NDC code
31722-726-30
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1213-2018

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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