US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 17, 2015 (11 years ago)

Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b) 500 count bottle…

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

Why it was recalled

Failed Stability Specifications: product may not meet specification limit for assay test.

What was recalled

Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b) 500 count bottle, Rx Only, Manufactured by: Apotex Research Pvt., Ltd., Bangalore, India, Manufactured for: Apotex Corp, Westin, FL, a) NDC 60505-3145-1, b) NDC 60505-3145-5

Recalling firm
Apotex Inc.
NDC code
60505-3145-1
Origin
Canada
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1814-2015

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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