The Procter & Gamble Company: Drug Recall

Recall #D-0253-2024 · 11/23/2021

Class II: Risk

Recall Details

Recall Number
D-0253-2024
Classification
Class II
Product Type
Drug
Recalling Firm
The Procter & Gamble Company
Status
Terminated
Date Initiated
11/23/2021
Location
Cincinnati, OH, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
unknown

Reason for Recall

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

Product Description

Secret, powder fresh, (Aluminum chlorohydrate 24%), Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 Topical spray cans, each can Net Wt. 6OZ (170g), NDC: 37000-134-01, UPC 0 37000 58690 6; Dist. by: Procter & Gamble, Cincinnati, OH 45202,

Distribution Pattern

Nationwide USA and Puerto Rico, Canada, Guam, Northern Mariana Islands, American Samoa, Bhutan, Timor-Leste, Maldives, Fiji, US Virgin Islands, Trinidad, Peru, Saint Marteen, Bahamas, Costa Rica, Guatemala, Honduras, Panama, Belize, Santa Lucia, Aruba, Dominican Republic, Guyana

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.