Protex Foaming Hand Sanitizer recalled over manufacturing violations
- Recall date
- August 2, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Parker Laboratories, Inc. recalls Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC 30775-040-0…
- Recall number
- D-1089-2023
- FDA classification
- Class II
- Brand / firm
- Parker Laboratories, Inc.
- Sold / distributed
- Nationwide within the United States, Singapore, Korea and Hong Kong
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC 30775-040-02) and b)18 fl. oz./550 ml Pump Bottles (NDC 30775-040-18), Parker Laboratories, Inc. 286 Eldridge Road, Fairfield, NJ 07004
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