PlainRecalls
FDA Drug Moderate Class II Terminated

deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.

Reported: November 14, 2018 Initiated: October 26, 2018 #D-0220-2019

Product Description

deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.

Reason for Recall

CGMP Deviations: Product was released to market prior to microbiological testing.

Details

Recalling Firm
S.C. Johnson Professional
Units Affected
869 cases
Distribution
NC
Location
Charlotte, NC

Frequently Asked Questions

What product was recalled?
deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.. Recalled by S.C. Johnson Professional. Units affected: 869 cases.
Why was this product recalled?
CGMP Deviations: Product was released to market prior to microbiological testing.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 14, 2018. Severity: Moderate. Recall number: D-0220-2019.