US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 22, 2019 (7 years ago)

AQUACIL instant foaming hand sanitizer, alcohol free formula, benzalkonium chloride 0.1%…

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

Why it was recalled

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

What was recalled

AQUACIL instant foaming hand sanitizer, alcohol free formula, benzalkonium chloride 0.1% (w/w), packaged in a) 18 FL OZ (532 mL) bottles, 12/18OZ bottles per case, Product Code BIO-5075-432-02; b) 1000 ML pouches, 6/1000 ML pouches per case, Product Code BIO575-OS1000, Biocentris Pharmaceuticals (Division of Inopak).

Recalling firm
Inopak Ltd
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1311-2019

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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