US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 24, 2016 (10 years ago)

Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule contains…

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

Why it was recalled

CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures

What was recalled

Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Methylene Blue, 10 mg; Hyoscyamine Sulfate, 0.12 mg, 100 count, Rx only, Manufactured for: BUREL PHARMACEUTICALS, NDC 35573-315-10

Recalling firm
Burel Pharmaceuticals Inc
NDC code
35573-315-10
Origin
MS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0160-2017

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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