HIGH

Doctor D. Schwab Pain Relief Gel Recalled Due to CGMP Violations

Doctor D. Schwab recalled 810 tubes of Clinical Weh Weh Natural Pain Relief Gel on October 10, 2025. The recall stems from CGMP deviations that could compromise product safety. The affected product was distributed in California, Colorado, Florida, Puerto Rico, and Washington.

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
WEH-WEH PAIN RELIEVER GEL, 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, Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel, contains 5% menthol and 4.2 oz. per tube. It is identified by NDC: 35192-020-02 and was sold in various states including CA, CO, FL, PR, and WA.

The Hazard

The recall is due to deviations from Current Good Manufacturing Practices (CGMP). These deviations can result in quality issues, potentially leading to compromised safety for consumers.

Reported Incidents

There are no reported injuries or incidents associated with this recall. Despite the lack of reported harm, the high hazard level indicates potential risks.

What to Do

Consumers should stop using the recalled product immediately. Contact CA BOTANA International, Inc. or consult a healthcare provider for further guidance.

Contact Information

For more information, consumers can visit the FDA website or contact CA BOTANA International, Inc. directly.

Key Facts

  • 810 tubes recalled
  • Contains 5% menthol
  • Distributed in CA, CO, FL, PR, WA
  • Stop using immediately
  • Contact CA BOTANA for guidance

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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot D53081
exp 7/31/2026
UPC Codes
35192-020
35192-020-02
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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