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deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge pack...

FDA Recall #D-0220-2019 — Class II — October 26, 2018

Recall #D-0220-2019 Date: October 26, 2018 Classification: Class II Status: Terminated

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.

Recalling Firm

S.C. Johnson Professional — Charlotte, NC

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

869 cases

Distribution

NC

Code Information

Lot 9131

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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