Quick Facts at a Glance
- Recall Date
- December 26, 2025
- Hazard Level
- HIGH
- Brand
- GOLD STAR DISTRIBUTION
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- GOLD STAR DISTRIBUTION
- Product type
- Alka Seltzer
- Model numbers
- All lots within expiry distributed by Gold Star Distribution.
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 26, 2025
Reported by FDA DRUG
January 21, 2026
RecallRadar source check
January 28, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact GOLD STAR DISTRIBUTION INC or your healthcare provider for guidance. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
Alka Seltzer is an over-the-counter medication commonly used to relieve symptoms of heartburn, indigestion, and cold and flu symptoms. Consumers typically buy it for quick relief from discomfort and to alleviate cold symptoms.
Why This Is Dangerous
The hazard arises from insanitary conditions, specifically rodent exposure, which poses a risk of contamination and illness. Contaminated products can lead to serious health issues if ingested.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers are urged to stop using the affected products immediately to avoid potential health risks. The recall may cause inconvenience as users seek alternative medications.
Practical Guidance
How to identify if yours is affected
- Verify if your product matches the recalled Alka Seltzer Original or Plus Cold & Flu formulations.
- Look for any notifications from Gold Star Distribution regarding the recall.
Where to find product info
The UPC codes can usually be found on the outer packaging of the product or inside the box.
What timeline to expect
Expect a refund processing timeline of approximately 4 to 6 weeks.
If the manufacturer is unresponsive
- Document your attempts to contact the company.
- Reach out to the FDA or consumer protection agencies for assistance.
- Consider filing a complaint with the Consumer Product Safety Commission.
How to prevent similar issues
- Look for products with clear labeling and packaging integrity.
- Check for recalls and safety notices before purchasing over-the-counter medications.
- Always review the manufacturing and expiration dates on medications.
Documentation advice
Keep a record of any correspondence with Gold Star Distribution, including dates and details of your inquiries.
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Product Details
The recall includes Alka Seltzer Original in 58 count boxes (UPC: 815556020033, 016500514473) and Alka Seltzer Plus Cold & Flu in 36 count boxes (UPC: 016500594932). These products were distributed nationwide in the United States.
Key Facts
- Recall date: December 26, 2025
- Reported date: January 21, 2026
- Class II recall due to insanitary conditions
- No injuries reported
- Products distributed nationwide
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Safety Guide
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