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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Simex Logistics SA de CV: Various Hand Sanitizers Recalled Due to Subpotency

Agency Publication Date: December 16, 2020
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Summary

Approximately 94,472 bottles of various brands of hand sanitizer, including +Protec Hands, CitruGel, Health & Hand, UVT World, and Lavar 70, are being recalled because they are subpotent. This means the products contain less than the required 70% alcohol antiseptic concentration, making them less effective at killing germs. These products were sold in sizes ranging from 33.8 ounces to 127.8 ounces and were distributed in California, Georgia, Nevada, and Texas.

Risk

Subpotent hand sanitizer may not effectively kill bacteria and viruses on the skin, potentially increasing the risk of infection when users rely on the product for germ protection.

What You Should Do

  1. Check your hand sanitizer bottles for the following brand names and identifying details: +Protec Hands (Lot 0-820, Exp 07/13/2023), CitruGel (Lot 0-620, Exp 06/10/2023), Health & Hand (Lot 0-720, Exp 05/16/2023), UVT World (Lot 0-620, Exp 08/05/2023), or Lavar 70 (Lot 0-520, Exp 05/26/2023).
  2. Look for the following barcodes: GOOD-GEL-04062020L, 0723707893163, 618149219889, 700306886772, or 7053335897.
  3. Stop using these specific lots of hand sanitizer immediately.
  4. Contact your healthcare provider or pharmacist for guidance regarding any concerns about ineffective germ protection.
  5. Return any unused product to the place of purchase for a refund and contact Simex Logistics SA de CV for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Drug recall refund process

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: +Protec Hands Antibacterial Gel Topical Solution Instant Sanitizer Hands 70% Alcohol Antiseptic (33.8 Oz / 1000mL)
Model:
D-0160-2021
Lot Numbers:
0-820 (Exp 07/13/2023)
Product: +Protec Hands Antibacterial Gel Topical Solution Instant Sanitizer Hands 70% Alcohol Antiseptic (127.8 oz / 3780mL)
Model:
D-0160-2021
UPC Codes:
0723707893163
Lot Numbers:
0-820 (Exp 07/13/2023)
Product: CitruGel Hand Sanitizer Advanced Formula 70% Alcohol Fresh Lemon Scent (33.81 FL OZ / 1L)
Model:
D-0161-2021
NDC: 78247-002-01
Lot Numbers:
0-620 (Exp 06/10/2023)
Product: Health & Hand Gel Hand Sanitizer 70% Alcohol Content (33.8 FL OZ / 1L)
Model:
D-0162-2021
UPC Codes:
618149219889
Lot Numbers:
0-720 (Exp 05/16/2023)
Product: UVT World Gel Hand Sanitizer 70% Alcohol Content (33.9 FL OZ / 1LT)
Model:
D-0163-2021
UPC Codes:
700306886772
Lot Numbers:
0-620 (Exp 08/05/2023)
Product: Lavar 70 Gel Hand Sanitizer 70% Alcohol Content (33.8 FL OZ / 1L)
Model:
D-0164-2021
UPC Codes:
7053335897
Lot Numbers:
0-520 (Exp 05/26/2023)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86858
Status: Resolved
Manufacturer: Simex Logistics SA de CV
Sold By: PS Promotional Services LLC; Citru Gel Inc.; Blue Ridge Southern Supply, LLC; UVT World
Manufactured In: Mexico
Units Affected: 5 products (19340 bottles; 1800 bottles; 19008 bottles; 16308 bottles; 38016 bottles)
Distributed To: California, Georgia, Nevada, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.