Clearasil Rapid Rescue Deep Treatment Pads — Class III drug recall D-1179-2023
Terminated recall by RB Health (US) LLC, reported 2023-10-04, distributed nationwide. Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
| Recall number | D-1179-2023 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RB Health (US) LLC, Parsippany, NJ, United States |
| Recall initiated | 2023-08-29 |
| Classified | 2023-09-27 |
| Reported by FDA | 2023-10-04 |
| Terminated | 2025-04-22 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, potency |
| NDC | 63824-0431, 63824-0431-90 |
| Lot numbers | KT220211 |
| Expiration dates | 2024-07 |
Product
Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in case of 6 jars per case, Distributed by RB Health (US), Parsippany, NJ 07054, NDC 63824-431-90
Reason for recall
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
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-1179-2023. 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.