Hyolev MB URINARY ANTISEPTIC Tablets recalled over manufacturing violations
- Recall date
- October 24, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Burel Pharmaceuticals Inc recalls Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral administration contains: Hyoscyamine Sulfate 0.12 mg, Methen…
- Recall number
- D-0155-2017
- FDA classification
- Class II
- Brand / firm
- Burel Pharmaceuticals Inc
- Sold / distributed
- Nationwide
Why it was recalled
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral administration contains: Hyoscyamine Sulfate 0.12 mg, Methenamine 81 mg, Methylene Blue 10.8 mg, Phenyl Salicylate 32.4 mg, Sodium Phosphate Monobasic 40.8 mg, 90 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-301-90
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