US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Dec 1, 2020 (6 years ago)

Zapien Productos Hand Sanitizer Gel Antibacterial, 33.8 FL. OZ (1000 mL), Made by GAZA…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP deviations: Product made at the same facility where product tested was sub-potent.

What was recalled

Zapien Productos Hand Sanitizer Gel Antibacterial, 33.8 FL. OZ (1000 mL), Made by GAZA S.A. DE C.V. Castilla St. #1473-A ZIP 45410 Tonala, Jalisco, Mexico, UPC: 7 501700 623504, NDC numbers: 76938-001-01, 76938-001-02, 76938-001-03.

Recalling firm
Gaza Proveedora De Servicios De Hospedaje Y Alimentacion
Origin
N/A, Mexico
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0230-2021

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.