ACURE — Class II drug recall D-0629-2018
Terminated recall by Diamond Wipes International, Inc., reported 2018-04-25, distributed nationwide. CGMP Deviations: finished products were manufactured with poor quality water.
| Recall number | D-0629-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Diamond Wipes International, Inc., Chino, CA, United States |
| Recall initiated | 2018-04-02 |
| Classified | 2018-04-16 |
| Reported by FDA | 2018-04-25 |
| Terminated | 2019-01-14 |
| Distributed | Nationwide (US) |
| Quantity | 51,840 pouches |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00854049003580 |
| Lot numbers | 01/19, 09/18, A106, A96, B106, C27 |
Product
ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.
Reason for recall
CGMP Deviations: finished products were manufactured with poor quality water.
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-0629-2018. 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.