WipeEssentials Wet Wipes — Class II drug recall D-0630-2018
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-0630-2018 |
|---|---|
| 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 | 5,148,792 pouches |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00766670039886 |
| Lot numbers | 03/18, 04/18, 05/18, 07/18, 08/18, 09/18, 7382A1, 7382A2, 7382A3, 7382B1, 7382B2, 7383A1, 7383A2, 7383B1, 7401A1, 7401B1, 7572A1, 7572B1, 7573A2, 7573B1, 7577A2, 7577B1, 7577B2, 7782A1, 7783A1, 7783B1, 7984A2, 7984B1, 7984B2, 8043A1, 8043B1, 8291A1, 8292B1, 8293A1, 8294B1, 8403A1, 8511A1, 8512B1, 8513A2, 8513B1 and 8 more |
Product
WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.
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-0630-2018. 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.