CLASS I Drug recall · Reported 11 May 2022 · FDA Enforcement Report

The Mandalorian Hand Sanitizer, ethyl alcohol recalled

Best Brands Consumer Products is recalling The Mandalorian Hand Sanitizer, ethyl alcohol 68%, Best Brands Consumer Products, Inc, distributed nationwide in the US. The recall was initiated on 29 Mar 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # 20E21, exp. date 09/30/2022
Quantity recalled346,320 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-0877-2022
FDA event ID
89802
Recalling firm
Best Brands Consumer Products, New York, NY
Classification
Class I
Status
Terminated
Recall initiated
29 Mar 2022
FDA classified
17 May 2022
Reported
11 May 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Benzene
Drug class
Hand Sanitizer

Timeline

29 Mar 2022Recall initiated by company
11 May 2022Published in enforcement report+43 days
17 May 2022Classified by FDA+6 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 product to contain benzene

Product as listed by the FDA

The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-012-02

Where it was distributed

Nationwide in the US

Nationwide

Questions about this recall

Why was it recalled?

Chemical Contamination; FDA analysis found product to contain benzene

Which lots are affected?

Lot # 20E21, exp. date 09/30/2022

Where was it sold?

Nationwide in the US

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

1 other product · FDA event 89802

This product is part of a recall event; the main page for the event is Mickey Mouse Hand Sanitizer, ethyl alcohol 68%/to mL recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IMickey Mouse Hand Sanitizer, ethyl alcohol 68%/to mL recalledBest Brands Consumer ProductsOtherNationwide

More recalls from Best Brands Consumer Products

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IMickey Mouse Hand Sanitizer, ethyl alcohol 68%/to mL recalledBest Brands Consumer ProductsOtherNationwide