The Recall Desk

FDA (Drugs) recall action 81453

S.C. Johnson Professional recalled 2 products on 2018-11-14

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2018-11-14
Critical
0
Units
1,127

Why these products were recalled

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

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–2 of 2

  • ModerateFDA (Drugs)··2018-11-14

    S.C. Johnson Recalls Deb Stoko Refresh AntiBac Foam Due to CGMP Deviations

    S.C. Johnson Professional is recalling 869 cases of Deb Stoko Refresh AntiBac Foam because the product was released to market before microbiological testing was completed.

    Product
    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.
    Category
    Distribution
    1 state
  • ModerateFDA (Drugs)··2018-11-14

    S.C. Johnson Recalls Alcohol-Free Foaming Hand Sanitizer Due to CGMP Deviations

    S.C. Johnson Professional is recalling 258 cases of Alcohol Free Foaming Hand Sanitizer because the product was released to market prior to microbiological testing.

    Product
    Alcohol Free Foaming Hand Sanitizer (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Safe-T-Fresh Inc., USA, 2530 Xenium Lane North, Minneapolis, MN 55441.
    Category
    Distribution
    1 state