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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.

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
Unknown
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
OTC Liquid Cold Medicine
Model numbers
All lots within expiry distributed by Gold Star Distribution.
Sold at
Unknown
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

    March 18, 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

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

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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

  • Hazard level: HIGH
  • Distribution scope: US Nationwide
  • Model scope: All lots within expiry distributed by Gold Star Distribution

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
POISONINGOTHER

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

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