Laboratorios Jaloma S.A. de C.V. recalls Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Oz. (1.06 pint, 500 mL),
Laboratorios Jaloma S.A. de C.V. recalls antiseptic hand sanitizer with 62% ethyl alcohol due to cGMP deviations. Products sold in Mexico with specific lot numbers and expiration dates.
Recall notice
cGMP deviations
Contact the company & request your remedy
What happened, in plain English
Laboratorios Jaloma S.A. de C.V. is recalling antiseptic hand sanitizer products in Mexico that failed quality control checks. This recall is due to cGMP deviations, which means the product may not meet safety standards. Read more at govinfonow.com/recall/36874-jaloma-antiseptic-hand-sanitizer-recall-cpg-deviations-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36874-jaloma-antiseptic-hand-sanitizer-recall-cpg-deviations-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1555-2020
Cite this page
“Jaloma Antiseptic Hand Sanitizer Recall: CPG Deviations Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36874-jaloma-antiseptic-hand-sanitizer-recall-cpg-deviations-risk. Based on FDA recall #D-1555-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1555-2020%22&limit=1).
Why it’s dangerous
The recall is for cGMP deviations, which are quality control failures in manufacturing. This means the product may not meet safety standards, but the specific risk to health is not clearly described in the notice.
Who’s affected
Owners of the recalled hand sanitizer products in Mexico are affected. Those using the product for hand hygiene are most at risk due to potential quality issues.
How to tell if you have this one
Check for the product name 'Jaloma Antiseptic Hand Sanitizer' with 62% ethyl alcohol and Vitamin E. Look for lot numbers 0005295, 0006373, 0005412, 0007134, 0007834, or 0009239, with expiration dates up to June 2022.
- Brand
Jaloma- Product
Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Oz. (1.06 pint, 500 mL)- Category
Drug
What to do — step by step
Check Product Details
Identify the product by checking the lot number and expiration date on the label.
Questions people ask
Why is this product being recalled?
The product failed quality control checks (cGMP deviations), but the specific health risk is not clearly described in the recall notice.
What should I do if I have this product?
The recall notice does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
Where was this product made?
The product was made in Mexico by Laboratorios Jaloma S.A. de C.V.
Contact Jaloma
We’ve drafted a message you can send Jaloma to request your refund or repair — edit it as you like.
Subject: Recall D-1555-2020 — Jaloma Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Hello, I own a Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Oz. (1.06 pint, 500 mL) that is covered by recall D-1555-2020 from Jaloma. 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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Where this comes from
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.
- Official source: FDA Recall #D-1555-2020 (July 31, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1555-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.