CLASS I Drug recall · Reported 24 Feb 2021 · FDA Enforcement Report

Optimus Lubricants Instant Hand Sanitizer, (ethyl alcohol 70%) recalled

Liq-E is recalling Optimus Lubricants Instant Hand Sanitizer, (ethyl alcohol 70%), distributed nationwide in the US. The recall was initiated on 20 Jul 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # (L)20-02, exp. date 05/2022
Quantity recalled12,201 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0253-2021
FDA event ID
86078
Recalling firm
Liq-E, San Nicolas De Los Georgia, N/A
Classification
Class I
Status
Terminated
Recall initiated
20 Jul 2020
FDA classified
12 Feb 2021
Reported
24 Feb 2021
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Other Reasons
Drug class
Hand Sanitizer

Timeline

20 Jul 2020Recall initiated by company
12 Feb 2021Classified by FDA+207 days
24 Feb 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Chemical Contamination: Products contain methanol and were below the label claim for ethanol content

Product as listed by the FDA

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

Where it was distributed

Distributed Nationwide in the United States and Mexico.

Nationwide

Questions about this recall

Why was it recalled?

Chemical Contamination: Products contain methanol and were below the label claim for ethanol content

Which lots are affected?

Lot # (L)20-02, exp. date 05/2022

Where was it sold?

Distributed Nationwide in the United States and Mexico.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 86078

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