CLASS I ONGOING Drug recall · Reported 8 Sep 2021 · FDA Enforcement Report

Medically Minded Hand Sanitizer Gel, Antimicrobial Formula recalled

Global Sanitizers is recalling Medically Minded Hand Sanitizer Gel, Antimicrobial Formula, (Ethyl Alcohol 70% v/v), distributed nationwide in the US. The recall was initiated on 12 May 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot No: E082020, "Best Buy": 5/21/2022
Quantity recalled50,000 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-0780-2021
FDA event ID
87941
Recalling firm
Global Sanitizers, Las Vegas, NV
Classification
Class I
Status
Ongoing
Recall initiated
12 May 2021
FDA classified
30 Aug 2021
Reported
8 Sep 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

12 May 2021Recall initiated by company
30 Aug 2021Classified by FDA+110 days
8 Sep 2021Published in enforcement report+9 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: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.

Product as listed by the FDA

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 FL OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC: 6 76753 00420 8,

Where it was distributed

Product Distributed Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.

Which lots are affected?

Lot No: E082020, "Best Buy": 5/21/2022

Where was it sold?

Product Distributed Nationwide in the USA

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

5 other products · FDA event 87941

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