Severity
Moderate
FDA Drug recall · Reported January 24, 2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
The Procter & Gamble Company recalled Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant… - a moderate-severity action.
Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant… was recalled by The Procter & Gamble Company in January 24, 2024. Reason: CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene. Check the official notice for the remedy. Verify recall #D-0251-2024 with the FDA Drug before acting.
The recall
The Procter & Gamble Company issued this moderate-severity FDA Drug recall-CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene.
Sourced from official FDA Drug enforcement records. Verify recall #D-0251-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0251-2024) was formally reported on January 24, 2024, with the manufacturer initiating the action on November 23, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. The Procter & Gamble Company is listed as the recalling firm, operating out of Cincinnati, OH. Federal records list the affected scope as unknown.
The documented reason for this recall is: CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene Distribution data in the federal record shows the product reached: 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, Pa…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
unknown
Related Recalls
6
5 from same agency
Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0251-2024 |
| Date reported | January 24, 2024 |
| Date initiated | November 23, 2021 |
| Recalling firm | The Procter & Gamble Company |
| Firm location | Cincinnati, OH |
| Affected scope | unknown |
| Distribution | 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 … |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported January 24, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.