Walgreens 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 Walgreens, NO DRIP, Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Original, 12 Hour, Maximum Stren…
- Recall number
- D-0063-2019
- 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
Walgreens, NO DRIP, Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Original, 12 Hour, Maximum Strength, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015,NDC 0363-7005-01, UPC 3 11917 18537 8.
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