The Recall Desk

FDA (Drugs) recall action 90756

Midlab Incorporated recalled 2 products on 2022-08-31

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
2022-08-31
Critical
0
Units
—

Why these products were recalled

CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

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

1–2 of 2

  • ModerateFDA (Drugs)··2022-08-31

    Maxim Instant Foam Hand Sanitizer recalled due to expired active ingredient

    Midlab Incorporated is recalling Maxim Instant Foam Hand Sanitizer nationwide. The product was manufactured using expired benzalkonium chloride, potentially compromising effectiveness.

    Product
    Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303
    Category
    Distribution
    0 states
  • HighFDA (Drugs)··2022-08-31

    Hand sanitizer recalled for use of expired active ingredient

    Corsair Personal Care 99X Instant Foam Hand Sanitizer is being recalled due to a manufacturing violation: it was made using expired benzalkonium chloride. Consumers should stop using the affected product.

    Product
    Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028
    Category
    Distribution
    0 states