FDA recall record

Medicis Pharmaceutical CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit recall — FDA D-916-2013

cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy

Class IIclassification
D-916-2013official record ID
Aug 28, 2013report date

Recall record at a glance

Official recordD-916-2013
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedicis Pharmaceutical Corp
Report dateAug 28, 2013
Recall initiation dateMay 1, 2013
Quantity2491 Kits; Expanded 8/29/2013 to include an additional 907 units.
LocationScottsdale, AZ, United States

Official product description

CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit, Distributed by OMP, Inc., Long Beach, CA 90806, Kit is comprised of: Daily Care Foaming Cleanser (Salicylic Acid 2%) NDC 62032-111; Pore Therapy (Salicylic Acid 2%) NDC 62032-110 and Therapeutic Lotion (Benzoyl Peroxide 5%) NDC 562032-113). Product under recall is the Pore Therapy (Salicylic Acid 2%), NDC 62032-110.

Why the product was recalled

cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy

Distribution information

Nationwide, Great Britain, Mexico, Russia and The Ukraine.

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

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