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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

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

Related Recalls

HIGH

Novo Nordisk Recalls Wegovy Injection Due to Contamination Risk

Novo Nordisk recalled Wegovy (semaglutide) Injection on December 19, 2025, due to hair found in a prefilled syringe. The recall affects products distributed nationwide in the United States. Consumers should stop using the product immediately and contact their healthcare provider.

Wegovy
Presence of
Read more
HIGH

Zydus Pharmaceuticals Recalls TraZODONE Tablets Over Defects

Zydus Pharmaceuticals recalled over 2,100 bottles of TraZODONE Hydrochloride Tablets on December 19, 2025. Some tablets have surface dents that may affect medication integrity. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Zydus Pharmaceuticals
Failed Tablet/Capsule
Read more
HIGH

Merck Recalls Noxafil Oral Suspension Due to Metal Contamination

Merck Sharp & Dohme LLC recalled 845 kits of Noxafil Powdermix on December 12, 2025. The recall follows the discovery of potential metal particulates in the product. Consumers should stop using the medication immediately and contact their healthcare provider for further guidance.

NOXAFIL
Presence of
Read more
HIGH

Merck Emend Recalled Due to Potential Metal Contamination

Merck Sharp & Dohme LLC recalled 3 single-dose kits of Emend (aprepitant) on December 12, 2025. The recall stems from the potential presence of metal particulates in the medication. Consumers should immediately stop using the product and contact their healthcare provider for guidance.

EMEND
Presence of
Read more
HIGH

Beaver-Visitec Recalls Laser and Endoscopy System Over Safety Hazard

Beaver-Visitec International recalled five units of the OME6000U Laser and Endoscopy System on December 5, 2025. The recall stems from a manufacturing deviation where ferrites required for the USB cable were not installed. This omission poses a high electrical hazard risk to patients and healthcare providers.

Beaver-Visitec International
Manufacturing deviation
Read more