AMERICA'S ORIGINAL DUBBLE BUBBLE SCENTED ANTIBACTERIAL HAND GEL — Class III drug recall D-1546-2019
Terminated recall by NingBo Huize Commodity Co.,Ltd., reported 2019-08-07. CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products
| Recall number | D-1546-2019 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | NingBo Huize Commodity Co.,Ltd., Yuyao, N/A, China |
| Recall initiated | 2019-04-01 |
| Classified | 2019-07-27 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2023-06-06 |
| Countries outside the US | CN |
| Quantity | 20,160 |
| Reason classes | cgmp, specification failure |
| Lot numbers | 20181106, 20181107 |
| Expiration dates | 2020-11-05, 2020-11-06 |
Product
AMERICA'S ORIGINAL DUBBLE BUBBLE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
Reason for recall
CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
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-1546-2019. 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.