Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported February 24, 2021
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621
Chemical Contamination: Products contain methanol and were below the label claim for ethanol content
Liq-E S.a. De C.v. recalled OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bott… — a critical-severity action.
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bott… was recalled by Liq-E S.a. De C.v. in February 24, 2021. Reason: Chemical Contamination: Products contain methanol and were below the label claim for ethanol content. Check the official notice for the remedy. Verify recall #D-0253-2021 with the FDA Drug before acting.
The recall
Liq-E S.a. De C.v. issued this critical-severity FDA Drug recall — Chemical Contamination: Products contain methanol and were below the label claim for ethanol content.
- Critical
- severity level
- Class I
- classification
- February 24, 2021
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0253-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0253-2021) was formally reported on February 24, 2021, with the manufacturer initiating the action on July 20, 2020. It is classified under Critical severity (Class I), with a current status of Terminated. Liq-E S.a. De C.v. is listed as the recalling firm, operating out of San Nicolas De Los Georgia, N/A. Federal records list the affected scope as 12,201 bottles.
The documented reason for this recall is: Chemical Contamination: Products contain methanol and were below the label claim for ethanol content Distribution data in the federal record shows the product reached: Distributed Nationwide in the United States and Mexico.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category — 3,146 children & baby products recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
12,201 bottles
Related Recalls
6
0 from same agency
Product description
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621
Reason for recall
Chemical Contamination: Products contain methanol and were below the label claim for ethanol content
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0253-2021 |
| Date reported | February 24, 2021 |
| Date initiated | July 20, 2020 |
| Recalling firm | Liq-E S.a. De C.v. |
| Firm location | San Nicolas De Los Georgia, N/A |
| Affected scope | 12,201 bottles |
| Distribution | Distributed Nationwide in the United States and Mexico. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0253-2021) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting — recall details can be updated.
- This is a Class I (high-risk) recall — stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621. Recalled by Liq-E S.a. De C.v.. Units affected: 12,201 bottles.
Why was this product recalled? ▼
Chemical Contamination: Products contain methanol and were below the label claim for ethanol content
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 24, 2021. Severity: Critical. Recall number: D-0253-2021.
Where was the recalled product distributed? ▼
Distribution: Distributed Nationwide in the United States and Mexico..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0253-2021) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported February 24, 2021.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.