Omega & Delta Co. recalls DOP Instant Hand Sanitizer with moisturizers due to inconsistent alcohol concentration. Products may not meet safety standards for effective hand cleaning. Affected lots include specific UPC and batch numbers.
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.
Omega & Delta Co. is recalling DOP Instant Hand Sanitizer bottles that may have lower than advertised alcohol content. This could mean the sanitizer isn't as effective at cleaning hands as it should be, potentially increasing infection risk.
The product was found to have inconsistent alcohol concentration during testing. This means some bottles may not contain enough alcohol to effectively kill germs on hands. The issue is related to manufacturing quality control, not the product's intended use.
People who own or use the recalled DOP Hand Sanitizer bottles with moisturizers. Those most at risk are individuals who rely on this product for frequent hand hygiene.
Check for the product name 'DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers', 4 fl oz bottle, and the lot numbers listed: 1327034, 1328034, 1277029, 1278029, 1202015, 1203015, 0246097, 0247097, 0247099, 0248099, 0252099.
Verify the product name, size, and lot numbers to confirm if your item is affected.
The product was found to have inconsistent alcohol concentration during testing, meaning some bottles may not meet the required strength for effective hand cleaning.
Check the lot numbers listed in the recall notice to see if your product is affected. If it is, you may want to consider using a different hand sanitizer.
The recall notice does not mention a specific remedy or fix for this product.
We’ve drafted a message you can send Omega & Delta to request your refund or repair — edit it as you like.
Subject: Recall D-0103-2024 — Omega & Delta Omega & Delta Hello, I own a Omega & Delta that is covered by recall D-0103-2024 from Omega & Delta. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
