Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated May 21, 2012 (14 years ago)

Hands Down Medicated Lotion Soap

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Presence of Undeclared Additive: Medicated lotion soap produced and distributed by the recalling firm contains the unapproved ingredient, Red Dye #15. This dye is not approved for use in food, drugs or cosmetics.

Cause type: Labeling / mix-up

Wrong label, wrong strength, mixed-up products, or packaging errors. One of the most dangerous causes - you can end up taking the wrong drug or the wrong dose. All labeling / mix-up recalls.

What was recalled

Hands Down Medicated Lotion Soap, 1 gallon bottle, 4 gallons per case, Distributed by PCS Industries, Crestwood, IL, 60446

Recalling firm
Kutol Products Co Inc
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1387-2012 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other labeling / mix-up recalls from 2012

All labeling / mix-up recalls
Class III · Low risk

Divalproex Sodium Delayed-Release Tablets

Labeling: Label Error On Declared Strength; Some bottles of product were missing the color-coded strength on the primary display panel of the label.

Terminated Labeling / mix-up Upsher Smith Laboratories, Inc. NDC 0245-0182-11 D-127-2013
Class III · Low risk

Bronkaid Dual Action Formula

Labeling: Label lacks warning or Rx legend; Certain information was inadvertently excluded from the product carton label.

Terminated Labeling / mix-up Bayer Healthcare, LLC D-177-2013
Class II · Moderate risk

Synthroid (Levothyroxine Sodium)

Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.

Terminated Labeling / mix-up Abbott Laboratories NDC 0074-7069-90 D-107-2013