HIGH

GOLD STAR DISTRIBUTION Vaporizing Chest Rub Recall 2026 All Lots Nationwide

Gold Star Distribution is recalling all lots of its Vaporizing Chest Rub, 4 oz, 12-count, UPC 048155903319, distributed nationwide in the United States. The recall, number D-0283-2026, stems from CGMP deviations including insanitary conditions with rodent exposure/activity at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star

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

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

Vaporizing Chest Rub is a topical product used for chest congestion relief. The recall covers a 4 oz, 12-count package distributed nationwide.

Why This Is Dangerous

CGMP deviations indicate insanitary conditions at the distribution center, including rodent exposure/activity. This creates potential contamination risk for the product.

Industry Context

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

Real-World Impact

No injuries reported. Consumers should avoid use until guidance is provided. Potential contamination risk warrants caution and prompt action.

Practical Guidance

How to identify if yours is affected

  1. Check packaging for Vaporizing Chest Rub, 4 oz, 12-count with UPC 048155903319
  2. Verify distributor as Gold Star Distribution
  3. Confirm lot is within expiry and distributed by Gold Star Distribution
  4. If in doubt, stop using the product and contact the distributor or healthcare provider

Where to find product info

FDA recall page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0283-2026

What timeline to expect

Refunds or replacements typically take several weeks after submission; follow updates from Gold Star Distribution

If the manufacturer is unresponsive

  • Escalate to FDA recall contacts or your state consumer protection office
  • Keep records of all communications
  • Consider filing a complaint with the CPSC if no resolution

How to prevent similar issues

  • Vet manufacturers for CGMP adherence before purchase
  • Check for recall notices on the FDA site and official distributor pages
  • Avoid purchasing from distributors with reported insanitary conditions
  • Keep packaging and receipts for records
  • Monitor for additional recall announcements

Documentation advice

Keep the product, packaging, UPC, batch/lot information, and all recall notices. Save correspondence with the distributor and any medical consultations.

Product Details

Product: Vaporizing Chest Rub Size: 4 oz Pack: 12-count UPC: 048155903319 Brand/Distributor: Gold Star Distribution Sold nationwide in the United States Model: All lots within expiry distributed by Gold Star Distribution Recall Date: 2025-12-26 Recall Number: D-0283-2026 Price: Unknown

Key Facts

  • Recall number D-0283-2026
  • UPC 048155903319
  • Product: Vaporizing Chest Rub, 4 oz, 12-count
  • All lots within expiry distributed by Gold Star Distribution
  • Distribution: US Nationwide
  • Hazard: CGMP deviations with insanitary conditions including rodent exposure in the distribution 中心

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
OTHER

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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