The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best
Summary
The FDA issued a Class I for The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best by Best Brands Consumer Products, Inc.. Reason: Chemical Contamination; FDA analysis found product to contain benzene.
Details
Source
Drug Recall
External ID
D-0877-2022
Action Date
2022-05-11
Status
Terminated
Category
drug
Product Description
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
Lot/Code Info: Lot # 20E21, exp. date 09/30/2022
Quantity Affected: 346,320 bottles
Reason for Recall
Chemical Contamination; FDA analysis found product to contain benzene
Distribution
Nationwide in the US
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-29
Company
New York, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 81 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Best Brands Consumer Products, Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Best Brands Consumer Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Best Brands Consumer Products, Inc. have FDA actions?
Best Brands Consumer Products, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0877-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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