Secret OUTLAST Dry Spray — Class II drug recall D-0248-2024
Terminated recall by The Procter & Gamble Company, reported 2024-01-24, distributed nationwide. CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
| Recall number | D-0248-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Procter & Gamble Company, Cincinnati, OH, United States |
| Recall initiated | 2021-11-23 |
| Classified | 2024-01-17 |
| Reported by FDA | 2024-01-24 |
| Terminated | 2024-10-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AW, BS, BZ, CA, CR, DO, GT, GY, HN, PA, PE, TT |
| Reason classes | chemical contamination, cgmp |
| UPC / GTIN / UDI-DI | 00037000747727 |
| NDC | 69423-0478-10 |
Product
Secret OUTLAST Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Protecting Powder, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-478-10, UPC 0 37000 74772 7
Reason for recall
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0248-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.