US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 26, 2013 (13 years ago)

Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva…

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

Why it was recalled

Failed Tablet/Capsule Specifications: There is a potential for broken tablets.

What was recalled

Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA, 18960, NDC 0093-7392-98

Recalling firm
Teva Pharmaceuticals USA
NDC code
0093-7392-98
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-396-2014

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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