Stop using now Drug recall · FDA · Published May 11, 2021

DiBAR LABS Hand Sanitizer Recall: Methanol Contamination Risk

DiBAR LABS recalls 8 oz hand sanitizer due to methanol contamination and low ethanol levels. Check your lot numbers immediately.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0644-2021Drug DiBAR LABS ›

Stop using this now

Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to be below the label claim for ethanol content and to contain methanol.

Take action

Contact the company

Recalling firmDIBAR NUTRICIONAL S DE RL DE CVSargento Manuel De La Rosa #145, Col Chapultepec Sur · Morelia, Mexico

✎ GovInfoNow plain-language explainer

DiBAR LABS is recalling specific lots of its 8 FL OZ Hand Sanitizer because FDA analysis found the products contained methanol and had less ethanol than labeled. Methanol is toxic if absorbed through the skin or ingested, posing a serious health risk. The recall covers products distributed nationwide in the USA. Read more at govinfonow.com/recall/36146-dibar-labs-hand-sanitizer-recall-methanol-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36146-dibar-labs-hand-sanitizer-recall-methanol-contamination-risk · Updated October 10, 2026 · FDA enforcement record: FDA #D-0644-2021

Cite this page

“DiBAR LABS Hand Sanitizer Recall: Methanol Contamination Risk.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/36146-dibar-labs-hand-sanitizer-recall-methanol-contamination-risk. Based on FDA recall #D-0644-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0644-2021%22&limit=1).

The FDA announced on May 11, 2021, that DiBAR NUTRICIONAL S DE RL DE CV voluntarily recalled DiBAR LABS Hand Sanitizer due to methanol contamination and ethanol levels below label claims. Owners should stop using the product immediately.

How to tell if you have it

DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL)
UPC 8 53090 00301 3
Lot # LDHSN050920 T1, LDHSN051020 DESC, LDHSN051020 T2
Expired May 2022

The hazard

FDA analysis found three lots of the hand sanitizer contained methanol and had ethanol content below the labeled 70 percent claim. The recall is classified as Class I, indicating a reasonable probability that use will cause serious adverse health consequences or death.

Context

GovInfoNow's records show other recent recalls of similar products include OneSource Specialty Pharma Methohexital Sodium Recall (2026-06-07) and Zep Alcohol Sanitizer Spray Recall (2026-05-22). Additional recent recalls include Haleon Gas-X Extra Strength Softgels Recall (2026-06-04).

How to tell if you have this one

Look for DiBAR LABS Hand Sanitizer in 8 FL OZ (236.5 mL) bottles with NDC 73009-0001-08 and UPC 8 53090 00301 3. Check the label for one of these lot numbers: LDHSN050920 T1, LDHSN051020 DESC, or LDHSN051020 T2. The expiration date on the bottle is 05/2022.

Brand
DiBAR LABS
Product
DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL), Distributed by S.E.N.D. LLC, Anthony, NM 88021
Category
Drug

FDA recall event · 4 products

All 4 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.

Status
Terminated
Distribution
Distributed Nationwide in the USA

Recall number	Product, codes & lots	Class
D-0644-2021	DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL), Distributed by S.E.N.D. LLC, Anthony, NM 88021, Imported by Dibar Labs, LLC, Sugar Land, TX 77479, Made in Mexico,77479, NDC 73009-0001-08 UPC 8 53090 00301 3.; Lot # LDHSN050920 T1, LDHSN051020 DESC, LDHSN051020 T2, EXP 05/2022	Class I
D-0645-2021	DiBAR LABS Hand Sanitizer, (ethyl alcohol 70%), packaged as a) 16 FL OZ (473.1 mL) bottle, NDC 73009-001-16, UPC 8 53090 00302 0 and b) 8 FL OZ (236.5 mL) bottle, NDC 73009-0001-08, UPC 8 53090 00301 3; Distributed by: S.E.N.D, LLC., Anthony, NM 88021; Imported by: Dibar Labs, LLC., Sugar Land, TX 77479, Made in Mexico.; All lots	Class II
D-0646-2021	ProtectoRx (ethyl alcohol 70%), packaged in a) 2 FL OZ (59 mL), NDC 75408-002-01 and b) 16 FL OZ (473.2 mL), NDC 75408-002-02 bottles, Imported by: Dibar Labs, LLC., Sugar Land, TX 77479; Distributed by: PR Trading LLC, PO Box 19647, San Juan, PR 00910, Made in Mexico.; All lots.	Class II
D-0647-2021	ADVANCE HAND SANITIZER, (ethyl alcohol 70%), 16 FL OZ (473.2 mL), Imported by: Dibar Labs, LLC,.Sugar Land, TX 77479, Distributed by: Lifetime Health Services, Pharr, TX 78577, Made in Mexico, NDC; 79284-005-00. UPC 8 60004 06470 1; All lots	Class II

Based on the official FDA remedy

What to do — step by step

Stop using the product
Do not use the recalled hand sanitizer due to the risk of methanol toxicity.
Discard or return the item
The record does not specify a return address or disposal method, so please dispose of it safely away from children and pets.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Distributed Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 22 months after the firm started it.

May 11, 2021Firm started the recall
Jun 29, 2021FDA classified it Class I
Jul 7, 2021Published in FDA’s Enforcement Report
Mar 8, 2023FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/36146-dibar-labs-hand-sanitizer-recall-methanol-contamination-risk">DiBAR LABS Hand Sanitizer Recall: Methanol Contamination Risk (GovInfoNow)</a>

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-0644-2021 (May 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0644-2021 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 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.