US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 22, 2017 (9 years ago)

Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber…

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

Why it was recalled

Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.

What was recalled

Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals. Inc. Piscataway, NJ 08854 By: HETERO, Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar-509 301, India. NDC 31722-708-30

Recalling firm
Hetero Labs Limited Unit V
NDC code
31722-708-30
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0415-2018

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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