Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 008
Summary
The FDA issued a Class I for Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged by TCP HRB ACQUISITON LLC. Reason: Chemical contamination: Presence of benzene.
Details
Source
Drug Recall
External ID
D-0207-2024
Action Date
2024-01-03
Status
Ongoing
Category
drug
Product Description
Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA
Lot/Code Info: All lots, expiry on or before August 2023
Quantity Affected: a) 0.4 million cans, b) 3.4 million cans
Reason for Recall
Chemical contamination: Presence of benzene
Distribution
Nationwide in the US and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-16
Company
Westport, CT
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 74 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
TCP HRB ACQUISITON LLC has 3 FDA actions in our database, including 3 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 (TCP HRB ACQUISITON LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TCP HRB ACQUISITON LLC have FDA actions?
TCP HRB ACQUISITON LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0207-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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