Blemfree All Day Lotion — Class II drug recall D-0591-2024
Terminated recall by Equibal Inc, reported 2024-07-17, distributed nationwide. CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
| Recall number | D-0591-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Equibal Inc, Unionville, NY, United States |
| Recall initiated | 2024-06-26 |
| Classified | 2024-07-09 |
| Reported by FDA | 2024-07-17 |
| Terminated | 2026-04-07 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00701450900086 |
| NDC | 53228-0002, 53228-0002-01, 53228-0003, 53228-0003-01 |
| Expiration dates | 2025-03-04, 2025-04-07 |
Product
Blemfree All Day Lotion (salicylic acid 0.5% w/w), packaged in a) 1 oz. 29 ML tube NDC:53228-003-01 b) 4 OZ 118ML plastic bottle, UPC 7 01450 90008 6, NDC # 53228-002-01, Equibal Labs, Inc
Reason for recall
CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
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-0591-2024. 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.