FDA recall record

REFRESH ANTIBAC FOAM deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L recall — FDA D-0220-2019

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

Class IIclassification
D-0220-2019official record ID
Nov 14, 2018report date

Recall record at a glance

Official recordD-0220-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmS.C. Johnson Professional
Report dateNov 14, 2018
Recall initiation dateOct 26, 2018
Quantity869 cases
LocationCharlotte, NC, United States

Official 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.

Why the product was recalled

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

Distribution information

NC

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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