Zeco LLC recalls 75% isopropyl alcohol hand sanitizer due to sterile water not used in production. Affected products include 1-gallon jugs, 5-gallon pails, and larger containers with specific lot numbers and expiration dates.
CGMP Deviations: sterile water not used for production
Zeco LLC is recalling their HAND-I-SAN hand sanitizer because it was made without sterile water, which could lead to contamination. This recall affects specific lot numbers and sizes of the product.
The recall is due to CGMP deviations where sterile water was not used in the production process. This could result in contamination of the product, potentially leading to health risks if the sanitizer is used improperly.
People who own or use the recalled HAND-I-SAN hand sanitizer products, including those with specific lot numbers and container sizes. The risk is highest for individuals using the product for hygiene purposes.
Check for the product name 'HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol)' with specific container sizes (1-gallon jugs, 5-gallon pails, etc.) and lot numbers listed in the expiration dates provided.
Identify the product by checking the container size and lot number on the label.
If you have the recalled product, stop using it immediately to avoid potential contamination risks.
The hazard is that sterile water was not used in the production process, which could lead to contamination.
The affected products include 1-gallon jugs, 5-gallon pails, and larger containers with specific lot numbers and expiration dates listed in the recall notice.
Check the product label for the specific container sizes and lot numbers provided in the recall notice.
We’ve drafted a message you can send Zeco to request your refund or repair — edit it as you like.
Subject: Recall D-0640-2024 — Zeco Zeco Hello, I own a Zeco that is covered by recall D-0640-2024 from Zeco. 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.
