Parker Laboratories recalls Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) due to CGMP deviations. Products sold in 2 fl oz/60 mL and 18 fl oz/550 mL pump bottles with specific lot numbers are affected.
CGMP Deviations
Parker Laboratories is recalling Protex Foaming Hand Sanitizer products that were manufactured with CGMP deviations. This recall is important because it addresses potential quality control issues that could affect product safety.
CGMP deviations refer to failures in the manufacturing process that may result in product quality issues. However, the recall does not specify the exact nature of the deviations or how they could cause harm.
Owners of Protex Foaming Hand Sanitizer products with specific lot numbers and sizes are affected. People using these products for hand hygiene are most at risk if they have the recalled items.
Check for the product name 'Protex Foaming Hand Sanitizer' in 2 fl oz/60 mL or 18 fl oz/550 mL pump bottles. Look for lot numbers G0323002 (expiring 3/1/2025) or G1122001 (expiring 11/15/2024).
Identify the lot number and expiration date on the product label to determine if it is part of the recall.
The recall states there were CGMP deviations, but does not specify the exact hazard or how it could cause harm.
The recalled products are Protex Foaming Hand Sanitizer in 2 fl oz/60 mL pump bottles (lot G0323002, expiring 3/1/2025) and 18 fl oz/550 mL pump bottles (lot G1122001, expiring 11/15/2024).
The recall does not specify a stop-use instruction, so there is no immediate action required beyond checking the product details.
We’ve drafted a message you can send Parker Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-1089-2023 — Parker Laboratories Parker Laboratories Hello, I own a Parker Laboratories that is covered by recall D-1089-2023 from Parker Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
