HIGH

Gold Star Distribution Recalls Liquid DayQuil 12/8oz for CGMP Issues (2025)

Gold Star Distribution is recalling Liquid DayQuil 12/8oz distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions, including rodent exposure at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

Quick Facts at a Glance

Recall Date
December 26, 2025
Hazard Level
HIGH
Brand
Gold Star Distribution
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

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

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About This Product

Liquid DayQuil is an OTC daytime cold remedy sold in 8 oz bottles as part of a 12-pack configuration.

Why This Is Dangerous

CGMP deviations indicate insanitary distribution conditions, including rodent exposure, which may contaminate products.

Industry Context

This recall is not stated as part of a broader industry pattern.

Real-World Impact

Consumers may be exposed to contaminated or compromised medication. Stop use immediately and follow recall guidance.

Practical Guidance

How to identify if yours is affected

  1. Verify product is Liquid DayQuil 12/8oz distributed by Gold Star Distribution
  2. Check expiry date and lot information on packaging
  3. Cross-check with FDA recall page linked in the notice

Where to find product info

FDA enforcement report D-0268-2026 and Gold Star Distribution contact information

What timeline to expect

Refund or replacement processes are not detailed; typical timelines range 4-6 weeks

If the manufacturer is unresponsive

  • Document all communication attempts with Gold Star Distribution
  • File a complaint with FDA or state consumer protection if the distributor is unresponsive
  • Keep records of correspondence and packaging images

How to prevent similar issues

  • Buy medicines from reputable retailers; verify CGMP compliance
  • Register for recall notifications from FDA and retailers
  • Check packaging for lot numbers and expiry dates before use

Documentation advice

Keep recall notice, packaging, receipts, and all correspondence with the distributor for records

Product Details

Product: LIQUID DAYQUIL 12/8oz Brand: Gold Star Distribution Model numbers: All lots within expiry distributed by Gold Star Distribution. Sold at: Unknown Date sold: Unknown Price: Unknown

Key Facts

  • Recall initiated 2025-12-26
  • Status: ACTIVE
  • Hazard level: HIGH
  • Distribution scope: US Nationwide
  • Model scope: All lots within expiry distributed by Gold Star Distribution
View Original Recall on FDA - Drug Safety

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Safety Guide

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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
POISONINGOTHER

Product Classification

Product TypeOTC Liquid Cold Medicine
Sold At
Unknown

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

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