Midlab recalls Maxim Instant Foam Hand Sanitizer made with expired benzalkonium chloride. This could cause harm if used. Affected units include specific UPCs and lots. Stop using immediately.
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Midlab is recalling Maxim Instant Foam Hand Sanitizer due to expired active ingredient. Using this product could pose a health risk because the ingredient may not work as intended.
The hand sanitizer was made using an expired active ingredient, benzalkonium chloride. This could mean the product doesn't work properly and might not protect against germs.
People who own or use the recalled Maxim hand sanitizer in the U.S. are affected. Those using the product for hand hygiene are most at risk.
Check for the product name 'Maxim Instant Foam Hand Sanitizer' in 1 U.S. Gallon drums with UPC 7 61841 02502 6 or 55 U.S. Gallon drums with UPC 0 07 61841 02504 0. Also check the lot numbers listed in the recall notice.
Discard the recalled hand sanitizer immediately as it contains an expired ingredient that may not be safe.
The product was manufactured using an expired active ingredient, benzalkonium chloride, which could affect its safety and effectiveness.
The recalled products include Maxim Instant Foam Hand Sanitizer in 1 U.S. Gallon drums with UPC 7 61841 02502 6 and 55 U.S. Gallon drums with UPC 0 07 61841 02504 0.
Check the UPC codes and lot numbers listed in the recall notice: 1 U.S. Gallon drums with UPC 7 61841 02502 6 and 55 U.S. Gallon drums with UPC 0 07 61841 02504 0, along with specific lot numbers.
We’ve drafted a message you can send Midlab to request your refund or repair — edit it as you like.
Subject: Recall D-1463-2022 — Midlab Midlab Hello, I own a Midlab that is covered by recall D-1463-2022 from Midlab. 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.
