HIGH

Colgate and Crest Toothpaste Recall 2025 by Gold Star Distribution for CGMP Deviations

Gold Star Distribution Inc. issued a nationwide recall of Colgate and Crest toothpaste on December 26, 2025 after inspectors found insanitary conditions and rodent exposure at its distribution center. The issue stems from CGMP deviations that could contaminate products. Consumers should stop using the affected toothpaste immediately and contact Gold Star Distribution for guidance.

Quick Facts at a Glance

Recall Date
December 26, 2025
Hazard Level
HIGH
Brands
Colgate, Crest, 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

Toothpaste is a daily-use oral care product manufactured by major brands Colgate and Crest. It is distributed nationwide and used in households for cleaning and whitening.

Why This Is Dangerous

The recall cites CGMP deviations with insanitary conditions and rodent exposure at the distribution center. This could lead to contamination of toothpaste batches.

Industry Context

This recall is not described as part of a broader industry pattern in the provided notice.

Real-World Impact

Consumers may need to stop using affected toothpaste promptly. The recall process involves refunds or replacements, with no reported injuries to date.

Practical Guidance

How to identify if yours is affected

  1. Check UPCs listed in the recall notice against your toothpaste packaging.
  2. Compare product name and package size to the affected lots.
  3. Inspect distributor and batch information on the product and packaging.

Where to find product info

UPC codes and packaging details are the primary identifiers. UPC numbers appear on the product barcode label.

What timeline to expect

Refunds or replacements are typically processed within 4-8 weeks after verification.

If the manufacturer is unresponsive

  • Escalate to FDA recall channels or consumer protection offices if Gold Star Distribution is unresponsive.
  • Document all attempts to contact the company and preserve all packaging and receipts.

How to prevent similar issues

  • Buy toothpaste from reputable retailers with clear recall notices.
  • Check recall databases before purchasing new toothpaste.
  • Beware of product that lacks clear packaging or UPCs.
  • Verify distributor information on the packaging.

Documentation advice

Keep the recall notice, product packaging, UPCs, receipts, and any correspondence with the distributor.

Product Details

Colgate toothpaste variations distributed by Gold Star Distribution Inc. include whitening 2.5 oz (24 ct) UPC 035000511065; Regular 2.5 oz (24 ct) UPC 035000511058; Triple 2.5 oz (24 ct) UPC 035000512109; Mint Zing 24 ct 2.5 oz UPC 035000744609; Colgate MaxFresh Spicy Fresh Red Toothpaste 72 ct 150 g (UPC not provided); Crest toothpaste 40 ct 8.2 oz UPC 037000247081. All lots within expiry distributed by Gold Star Distribution are included. The recall is US nationwide. Sold through multiple retailers. Specific price and sale dates are not provided.

Key Facts

  • Recall date: 2025-12-26
  • Status: ACTIVE
  • Hazard level: HIGH
  • Incidents: 0 reported injuries or deaths
  • Manufacturer: Gold Star Distribution Inc
  • Brands involved: Colgate, Crest

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
7/ 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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