Rhinall Nasal Decongestant Nose Drops recalled over manufacturing violations
- Recall date
- August 3, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Product Quest Manufacturing LLC recalls Rhinall (phenylephrine hydrochloride) Nasal Decongestant Nose Drops, 0.25%, 1 FL OZ (30 mL) bottle, Distributed by: Sch…
- Recall number
- D-0028-2019
- FDA classification
- Class II
- Brand / firm
- Product Quest Manufacturing LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Rhinall (phenylephrine hydrochloride) Nasal Decongestant Nose Drops, 0.25%, 1 FL OZ (30 mL) bottle, Distributed by: Scherer Labs International, LLC., 330 Carswell Ave., Daytona Beach, FL 32117, UPC 3 02747 52531 1.
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