Asiaticon V-Klean Hand Sanitizer Gel 70% Recall: Lack of CGMPs
Asiaticon recalls V-Klean Hand Sanitizer Gel Alcohol 70% due to lack of current good manufacturing practices (CGMPs). Affected products include 250ml and 500ml bottles with specific UPCs. Consumers should contact the manufacturer for details.
Recall notice
Lack of CGMPs:
Contact the company
What happened, in plain English
Asiaticon is recalling V-Klean Hand Sanitizer Gel Alcohol 70% products because they were made without proper current good manufacturing practices (CGMPs). This could mean the product isn't safe for use as intended. Read more at govinfonow.com/recall/36800-asiaticon-v-klean-hand-sanitizer-gel-70-recall-lack-of.
Source Summary by GovInfoNow · govinfonow.com/recall/36800-asiaticon-v-klean-hand-sanitizer-gel-70-recall-lack-of · Updated October 4, 2026 · FDA enforcement record: FDA #D-0116-2021
Cite this page
“Asiaticon V-Klean Hand Sanitizer Gel 70% Recall: Lack of CGMPs.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36800-asiaticon-v-klean-hand-sanitizer-gel-70-recall-lack-of. Based on FDA recall #D-0116-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0116-2021%22&limit=1).
Why it’s dangerous
The product was made without following current good manufacturing practices (CGMPs), which are standards to ensure safety and quality. This could lead to the product being unsafe for use, but the exact risk isn't specified in the recall.
Who’s affected
Anyone who owns or uses the V-Klean Hand Sanitizer Gel Alcohol 70% products with the specified UPCs and sizes. People who rely on hand sanitizer for hygiene are most at risk.
How to tell if you have this one
Check for the product names V-Klean Hand Sanitizer Gel Alcohol 70% with sizes 250ml (8.5 fl oz) or 500ml (16.9 fl oz). The UPC numbers are 7 16053 70499 3 for both sizes.
- Brand
Asiaticon- Product
V-Klean Hand Sanitizer Gel Alcohol 70% packaged as a)8.5 fl oz (250 ml), UPC 7 16053 70499 3; b) 16.9 fl oz (500 ml)- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Distributed in Texas
| Recall number | Product, codes & lots |
|---|---|
| D-0116-2021 | V-Klean Hand Sanitizer Gel Alcohol 70% packaged as a)8.5 fl oz (250 ml), UPC 7 16053 70499 3; b) 16.9 fl oz (500 ml), UPC 7 16053 70499 3; c) 33.8 fl. oz. (1000 ml) bottles: 716053704993; Manufactured by: Asiaticon S.A. de C.V. Conkar 62, Jardines del Ajusco. Tlalpan Cuidad de Mexico. 14200 ;; All lots. |
| D-0117-2021 | Protz real protection Antibacterial Hand Sanitizer, Ethyl Alcohol 70%, 13.5 FL OZ (400 mL), Distributed by: Safety-Med Products, Inc. Burlington, WI 53105 Made in Mexico by Asiaticon S.A. de C.V. Conkal No. 62, Mexico, Ciudad de Mexico 14200, Mexico NDC: 75192-600-02 UPC 7 503019 005002; All lots. |
What to do — step by step
Contact Manufacturer
Reach out to Asiaticon, SA de CV at Conkar 62, Jardines del Ajusco, Tlalpan Ciudad de Mexico 14200 for specific instructions.
Where it went and when
Where it was distributed
Distributed in Texas.
FDA distribution: “Distributed in Texas” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Texas.
Recall timeline
FDA terminated this recall 2.7 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0116-2021 (August 25, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0116-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.