FDA recall record

Unilever United States Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent, Aluminum recall — FDA D-0211-2024

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

Class IIclassification
D-0211-2024official record ID
May 4, 2022report date

Recall record at a glance

Official recordD-0211-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmUnilever United States Inc.
Report dateMay 4, 2022
Recall initiation dateMar 30, 2022
Quantityunknown
LocationEnglewood Cliffs, NJ, United States

Official product description

Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent, Aluminum Chlorohydrate (19.1%), packaged in 6 oz. cans, Unilever, Dist. By Unilever, Trumbull, CT 06611 UPC 0 79400 78550 3

Why the product was recalled

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

Distribution information

Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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