RecallRadar

FDA Drug recall D-1311-2019

AQUACIL instant foaming hand sanitizer, alcohol free formula, benzalkonium chloride 0.1% (w/w), packaged in a) 18 FL OZ (532 mL) bottles, 1…

On 2019-06-05 the FDA classified a Class II recall of AQUACIL instant foaming hand sanitizer, alcohol free formula, benzalkonium chloride 0.1% (w/w), packaged in a) 18 FL OZ (532 mL) bottles, 1… by Inopak, citing CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1311-2019
ClassificationClass II
Statusterminated
Initiated2019-04-22
Published2019-06-05
Last updated2026-09-13 11:52 UTC
CompanyInopak
DistributionUS

Product

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).

Reason

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

Identifiers

code_infoBatch #: 6736, 6826

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-1311-2019%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.