FDA Drug recall D-1546-2019
AMERICA'S ORIGINAL DUBBLE BUBBLE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterpris…
- FDA Drug
- Class III
- terminated
- Published 2019-08-07
On 2019-08-07 the FDA classified a Class III recall of AMERICA'S ORIGINAL DUBBLE BUBBLE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterpris… by Ningbo Huize Commodity, citing CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1546-2019 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-04-01 |
| Published | 2019-08-07 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Ningbo Huize Commodity |
| Distribution | n/a |
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
CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
Identifiers
| code_info | Lot #: 20181106, Exp 11/5/2020; 20181107, Exp 11/6/2020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1546-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.