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Benadryl Recalled Due to Rodent Exposure Risk

Gold Star Distribution recalled Benadryl on December 26, 2025, due to insanitary conditions linked to rodent activity. The recall impacts all lots within expiry distributed by the company. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Official notice
GOLD STAR DISTRIBUTIONHealth & Personal CareDrugs & MedicationsAll lots within expiry distributed by Gold Star Distribution.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
December 26, 2025
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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
Antihistamine
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.

  1. Recall announced

    December 26, 2025

  2. Reported by FDA DRUG

    January 21, 2026

  3. RecallRadar source check

    January 28, 2026

  4. 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

Benadryl is an antihistamine commonly used to relieve symptoms of allergies and colds. Consumers purchase this product for its effectiveness in alleviating sneezing, runny nose, and itching.

Why This Is Dangerous

The recall is due to insanitary conditions at the distribution center, specifically rodent exposure, which can contaminate the product and pose serious health risks.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face health risks from using contaminated products. The recall necessitates immediate action to avoid potential harm.

Practical Guidance

How to identify if yours is affected

  1. Check the UPC number on the packaging.
  2. Verify if the product is within the expiry date.
  3. Ensure the product was distributed by Gold Star Distribution.

Where to find product info

The UPC code can typically be found on the bottom or back of the packaging.

What timeline to expect

Expect a refund processing time of 4-6 weeks.

If the manufacturer is unresponsive

  • Document all communications with the company.
  • Contact the FDA for further assistance.
  • Consider filing a complaint with the CPSC.

How to prevent similar issues

  • Look for products with clear safety certifications.
  • Research manufacturers' safety records before purchase.
  • Avoid purchasing products from unfamiliar distributors.

Documentation advice

Keep records of your purchase, including receipts, and any correspondence regarding the recall.

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Product Details

The recalled product is Benadryl, sold in 25's 2-pack boxes with UPC 815556020316. The product was distributed nationwide across the United States.

Key Facts

  • Recalled product: Benadryl, 25'S 2PK Box
  • Recall date: December 26, 2025
  • Class II recall due to insanitary conditions
  • Distributed nationwide in the US

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
GENERAL
Injury Types
POISONING

Product Classification

Product Details

Model Numbers
All lots within expiry distributed by Gold Star Distribution.
Affected States
ALL
Report Date
January 21, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

Gold Star Distribution Recalls Claritin Over Rodent Contamination

Gold Star Distribution recalled Claritin, 20 Count, on December 26, 2025, due to insanitary conditions resulting from rodent exposure. The recall affects an unknown quantity distributed nationwide. Consumers should stop using the product immediately.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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