Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) Recalled by Parker Laboratories, Inc. Due to CGMP Deviations
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Parker Laboratories, Inc. directly.
Affected Products
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
Quantity: 9
Why Was This Recalled?
CGMP Deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Parker Laboratories, Inc.
Parker Laboratories, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report