US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 28, 2016 (10 years ago)

Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only…

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

Why it was recalled

CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.

What was recalled

Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-701-10.

Recalling firm
Nationwide Laboratories, LLC
NDC code
42937-701-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0167-2017

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.

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