US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 18, 2017 (9 years ago)

Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila…

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

Why it was recalled

Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets

What was recalled

Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8

Recalling firm
Zydus Pharmaceuticals USA Inc
NDC code
68382-099-06
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1137-2017

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.

Other Paroxetine recalls

See all