US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 1, 2019 (7 years ago)

AMERICA'S ORIGINAL DUBBLE BUBBLE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.

What was recalled

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.

Recalling firm
NingBo Huize Commodity Co.,Ltd.
Origin
N/A, China
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1546-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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