US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 29, 2023 (3 years ago)

Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.

What was recalled

Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in case of 6 jars per case, Distributed by RB Health (US), Parsippany, NJ 07054, NDC 63824-431-90

Recalling firm
RB Health (US) LLC
NDC code
63824-431-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1179-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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