HIGH

CA Botana Recalls Doctor D. Schwab Cream Over Quality Issues

CA Botana International recalled 470 tubes of Doctor D. Schwab Controlling Cream on October 10, 2025. The recall stems from CGMP deviations that pose a high hazard risk. Consumers should stop using the product and seek guidance from healthcare providers.

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
CONTROLLING CREAM, CA-BOTANA INTERNATIONAL
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
5 states
At-Risk Groups
GENERAL

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for guidance. Notification method: Letter

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Product Details

The recalled product is Doctor D. Schwab Controlling Cream containing 2.7% Benzoyl Peroxide, packaged in 1 FL OZ (30 ML) tubes. It was distributed across California, Colorado, Florida, Puerto Rico, and Washington, and has a lot code of D54066 with an expiration date of May 31, 2027.

The Hazard

The recall was initiated due to CGMP deviations, indicating potential quality issues in the manufacturing process. While specific incident data is unavailable, the classification as a Class II recall suggests moderate risk to consumers.

Reported Incidents

No specific injuries or incidents have been reported in connection with this product. The nature of CGMP deviations raises concerns about product quality.

What to Do

Consumers and healthcare providers should stop using the recalled cream immediately. For further guidance, contact CA Botana International, Inc. or a healthcare provider. A notification letter will be provided to consumers.

Contact Information

For more information, consumers can visit the FDA recall page at www.accessdata.fda.gov or contact CA Botana International, Inc.

Key Facts

  • Recalled product: Doctor D. Schwab Controlling Cream
  • Quantity: 470 tubes
  • Hazard: CGMP Deviations
  • Stop using product immediately
  • Contact healthcare provider for guidance

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot Code D54066
exp 5/31/2027
UPC Codes
35192-017
35192-017-05
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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