The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0255-2021·Announced 2021-02-24

Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination

Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

The agency’s classification

FDA (Drugs): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.

Plain-English summary

Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer, 1-gallon bottles, due to chemical contamination. The product contains methanol and the ethanol content is below the level stated on the label.

The recalled product is identified by Lot # 20-03 and an expiration date of 05/22. A total of 6,597 gallons were distributed nationwide in the United States and Mexico.

Consumers should stop using the product and contact the recalling firm for instructions on how to return it or obtain a refund.

The recalled product

Product
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 1 Gal (3.78 L) 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; NDC: XXXXX-378-04, UPC # 7 501799 118837
Manufacturer
Liq-E S.A. De C.V.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot # (L) 20-03
  • exp. date 05/22

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 4 recalled by Liq-E S.A. De C.V. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →

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