CLASS I ONGOING Drug recall · Reported 3 Jan 2024 · FDA Enforcement Report
Brut Classic Antiperspirant & Deodorant recalled by Tcp Hrb Acquisiton
TCP HRB Acquisiton is recalling Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%), distributed nationwide in the US. The recall was initiated on 16 Feb 2022 and the FDA has classified it as Class I.
Check your package
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-0207-2024
- FDA event ID
- 89601
- Recalling firm
- TCP HRB Acquisiton, Westport, CT
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 16 Feb 2022
- FDA classified
- 28 Dec 2023
- Reported
- 3 Jan 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Benzene
- Drug class
- Sunscreen & Personal Care
Timeline
| 16 Feb 2022 | Recall initiated by company | |
| 28 Dec 2023 | Classified by FDA | +680 days |
| 3 Jan 2024 | Published in enforcement report | +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: Presence of benzene
Product as listed by the FDA
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
Where it was distributed
Nationwide in the US and Canada
Questions about this recall
Why was it recalled?
Chemical contamination: Presence of benzene
Which lots are affected?
All lots, expiry on or before August 2023
Where was it sold?
Nationwide in the US and Canada
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
2 other products · FDA event 89601This product is part of a recall event; the main page for the event is Sure Unscented Anti-perspirant Deodorant Aerosol recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Sure Unscented Anti-perspirant Deodorant Aerosol recalled | TCP HRB Acquisiton | Benzene | Nationwide | |
| CLASS I | Sure Regular Antiperspirant Deodorant Aerosol recalled | TCP HRB Acquisiton | Benzene | Nationwide |
More recalls from TCP HRB Acquisiton
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Sure Regular Antiperspirant Deodorant Aerosol recalled | TCP HRB Acquisiton | Benzene | Nationwide |
| Drug | CLASS I | Sure Unscented Anti-perspirant Deodorant Aerosol recalled | TCP HRB Acquisiton | Benzene | Nationwide |