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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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Critical RiskFDA Drug
Medications & Supplements/Topical Products

DiBAR LABS and ProtectoRx Hand Sanitizers Recalled for Methanol Contamination

Agency Publication Date: June 29, 2021
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Summary

Dibar Nutricional is recalling various hand sanitizers sold under the DiBAR LABS, ProtectoRx, and ADVANCE brands because they may contain methanol (wood alcohol). FDA testing discovered that some lots contained methanol instead of the expected ethyl alcohol and were below the required alcohol concentration. Although no injuries have been reported, methanol exposure can be toxic when absorbed through the skin or life-threatening if ingested.

Risk

Methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Consumers who have accidentally or intentionally ingested these products are at the highest risk for severe health consequences.

What You Should Do

  1. This recall affects DiBAR LABS, ProtectoRx, and ADVANCE HAND SANITIZER products sold in 2 oz, 8 oz, and 16 oz bottles.
  2. Check your product label for NDC codes 73009-0001-08, 73009-001-16, 75408-002-01, 75408-002-02, or 79284-005-00 and UPC codes including 853090003013 and 853090003020. See the Affected Products section below for the full list of affected codes.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
🗑️Option 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: DiBAR LABS Hand Sanitizer (8 FL OZ)
Variants: Ethyl Alcohol 70%, 236.5 mL
UPC Codes:
853090003013
Lot Numbers:
LDHSN050920 T1 (Exp 05/2022)
LDHSN051020 DESC (Exp 05/2022)
LDHSN051020 T2 (Exp 05/2022)
NDC:
73009-0001-08

Imported by Dibar Labs, LLC

Product: DiBAR LABS Hand Sanitizer (16 FL OZ)
Variants: Ethyl Alcohol 70%, 473.1 mL
UPC Codes:
853090003020
Lot Numbers:
All lots
NDC:
73009-001-16

Distributed by S.E.N.D, LLC

Product: ProtectoRx Hand Sanitizer (2 FL OZ)
Variants: Extra Strength, 59 mL
Lot Numbers:
All lots
NDC:
75408-002-01

Distributed by PR Trading LLC

Product: ProtectoRx Hand Sanitizer (16 FL OZ)
Variants: Extra Strength, 473.2 mL
Lot Numbers:
All lots
NDC:
75408-002-02

Distributed by PR Trading LLC

Product: ADVANCE HAND SANITIZER (16 FL OZ)
Variants: Ethyl Alcohol 70%, 473.2 mL
UPC Codes:
860004064701
Lot Numbers:
All lots
NDC:
79284-005-00

Distributed by Lifetime Health Services

Product Images

Dibar Labs Hand Sanitizer

Dibar Labs Hand Sanitizer

Dibar Labs Hand Sanitizer

Dibar Labs Hand Sanitizer

Image 1 - ProtectoRx Hand Sanitizer

Image 1 - ProtectoRx Hand Sanitizer

ProtectoRx Hand Sanitizer

ProtectoRx Hand Sanitizer

Dibar Labs Hand Sanitizer, 8 oz

Dibar Labs Hand Sanitizer, 8 oz

Dibar Labs Hand Sanitizer, 16 oz

Dibar Labs Hand Sanitizer, 16 oz

ProtectoRx Hand Sanitizer, 2 oz

ProtectoRx Hand Sanitizer, 2 oz

ProtectoRx Hand Sanitizer, 16 oz

ProtectoRx Hand Sanitizer, 16 oz

Advance Hand Sanitizer

Advance Hand Sanitizer

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87917
Status: Resolved
Manufacturer: DIBAR NUTRICIONAL S DE RL DE CV
Sold By: S.E.N.D. LLC; Dibar Labs, LLC; PR Trading LLC; Lifetime Health Services
Manufactured In: Mexico
Units Affected: 4 products (Unknown quantity; Unknown quantity; Unknown quantity; Unknown quantity)
Distributed To: Nationwide

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 · FDA Press Release (1) · FDA Press Release (2) · 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.