Suave 24-Hour Protection Aerosol Antiperspirant Powder scent, Aluminum Chlorohydrate (19.1%), packaged in a) 4 oz. cans
Summary
The FDA issued a Class I for Suave 24-Hour Protection Aerosol Antiperspirant Powder scent, Aluminum Chlorohyd by Unilever United States Inc.. Reason: Chemical contamination: presence of benzene.
Details
Source
Drug Recall
External ID
D-0210-2024
Action Date
2022-05-04
Status
Ongoing
Category
drug
Product Description
Suave 24-Hour Protection Aerosol Antiperspirant Powder scent, Aluminum Chlorohydrate (19.1%), packaged in a) 4 oz. cans (UPC 0 79400 75150 8), and b) 6 oz. cans (UPC 0 79400 78490 2), Dist. By Unilever, Trumbull, CT 06611
Lot/Code Info: all lots, expiry 9/30/2023
Quantity Affected: unknown
Reason for Recall
Chemical contamination: presence of benzene
Distribution
Nationwide in the US
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-30
Company
Englewood Cliffs, NJ
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 121 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Unilever United States 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 (Unilever United States Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Unilever United States Inc. have FDA actions?
Unilever United States 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-0210-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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