HIGH

Weh-Weh Pain Reliever Gel Recalled for CGMP Deviations, 810 Tubes Affected (2025)

CA BOTANA International recalled 810 tubes of Doctor D. Schwab Weh-Weh Natural Pain Relief Gel due to CGMP deviations. The recall covers tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. Consumers should stop using the product immediately and contact CA BOTANA for guidance.

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
Unknown
Geographic Scope
5 states
At-Risk Groups
GENERAL, PREGNANT, PETS

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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About This Product

Weh-Weh Pain Reliever Gel is a menthol-based topical analgesic marketed for temporary relief of minor aches and pains.

Why This Is Dangerous

CGMP deviations indicate manufacturing process issues that could affect product quality or safety, though no specific adverse events are reported here.

Industry Context

This recall is not identified as part of a broader industry pattern in the provided data.

Real-World Impact

Consumers may need to discard affected tubes and seek guidance from the manufacturer or a healthcare provider.

Practical Guidance

How to identify if yours is affected

  1. Check lot number on the tube label: Lot D53081
  2. Check expiration date: Exp 7/31/2026
  3. Verify NDC: 35192-020-02
  4. Compare product name and packaging to recall notice

Where to find product info

FDA enforcement page for recall D-0188-2026 and CA BOTANA communications

What timeline to expect

Remediation through recall notification letters; refunds or replacements to be arranged by manufacturer; typical processing time 4-8 weeks

If the manufacturer is unresponsive

  • Contact FDA consumer complaint coordinator
  • File a safety report with CPSC if applicable
  • Consider seeking legal advice if consumer rights are infringed

How to prevent similar issues

  • Buy CGMP-compliant products with clear labeling
  • Verify NDC against FDA list before use
  • Keep packaging and receipts for recalls
  • Monitor FDA recall updates and company notices

Documentation advice

Keep lot number, expiration date, photos of product and packaging, and recall communication

Product Details

Brand: WEH-WEH PAIN RELIEVER GEL. Manufacturer: CA BOTANA INTERNATIONAL, a division of CA BOTANA. Product: Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica. Menthol 5%. Size: 4.2 oz / 120 g per tube. NDC: 35192-020-02. Quantity: 810 tubes. Lot: D53081. Expiration: 7/31/2026. Distribution: CA, CO, FL, PR, WA.

Reported Incidents

No injuries or incidents have been reported in the provided records.

Key Facts

  • 810 tubes recalled
  • Lot D53081
  • Exp 7/31/2026
  • Menthol 5%
  • Distributed to CA, CO, FL, PR, WA
  • High-hazard CGMP deviation

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
ELECTRICALLACERATIONOTHER

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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