Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported August 28, 2013
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.
cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy
Medicis Pharmaceutical Corp recalled CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit, Distributed by OMP, Inc.… - a moderate-severity action.
CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit, Distributed by OMP, Inc.… was recalled by Medicis Pharmaceutical Corp in August 28, 2013. Reason: cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bott…. Check the official notice for the remedy. Verify recall #D-916-2013 with the FDA Drug before acting.
The recall
Medicis Pharmaceutical Corp issued this moderate-severity FDA Drug recall-cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bott….
- Moderate
- severity level
- Class II
- classification
- August 28, 2013
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-916-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-916-2013) was formally reported on August 28, 2013, with the manufacturer initiating the action on May 1, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Medicis Pharmaceutical Corp is listed as the recalling firm, operating out of Scottsdale, AZ. Federal records list the affected scope as 2491 Kits; Expanded 8/29/2013 to include an additional 907 units..
The documented reason for this recall is: 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 data in the federal record shows the product reached: Nationwide, Great Britain, Mexico, Russia and The Ukraine.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
2491 Kits; Expanded 8/29/2013 to include an additional 907 units.
Related Recalls
6
3 from same agency
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.
Reason for recall
cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-916-2013 |
| Date reported | August 28, 2013 |
| Date initiated | May 1, 2013 |
| Recalling firm | Medicis Pharmaceutical Corp |
| Firm location | Scottsdale, AZ |
| Affected scope | 2491 Kits; Expanded 8/29/2013 to include an additional 907 units. |
| Distribution | Nationwide, Great Britain, Mexico, Russia and The Ukraine. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-916-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Medicis Pharmaceutical Corp. Units affected: 2491 Kits; Expanded 8/29/2013 to include an additional 907 units..
Why was this product 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
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 28, 2013. Severity: Moderate. Recall number: D-916-2013.
Where was the recalled product distributed? ▼
Distribution: Nationwide, Great Britain, Mexico, Russia and The Ukraine..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-916-2013) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported August 28, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.