HIGHFDA DEVICE

PREGNANCY TEST 24CT

Potential exposure of rodents and rodent activity in the distribution center.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
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 - Medical Devices; 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
Pregnancy Test
Model numbers
UPC 048155920200
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 DEVICE

    February 4, 2026

  3. RecallRadar source check

    February 11, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Potential exposure of rodents and rodent activity in the distribution center.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact GOLD STAR DISTRIBUTION INC or your healthcare provider for instructions. Notification method: Press Release

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may experience inconvenience due to the recall and potential health risks associated with contamination.

Practical Guidance

How to identify if yours is affected

  1. Check the UPC number: 048155920200
  2. Verify the product packaging for recall notices
  3. Contact the retailer if unsure about the product's recall status

Where to find product info

UPC codes can typically be found on the packaging or printed on the product itself.

What timeline to expect

Expect 4 to 6 weeks for refund processing after contacting Gold Star Distribution.

If the manufacturer is unresponsive

  • Document all communications with Gold Star Distribution
  • Contact local consumer protection agencies for assistance
  • Consider filing a complaint with the FDA if no response is received

How to prevent similar issues

  • Look for FDA approval or clearance when purchasing medical devices
  • Check for recall history of products before buying
  • Purchase from reputable retailers to ensure product safety

Documentation advice

Keep receipts, correspondence with the company, and any product packaging for your records.

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Key Facts

  • Recall date: December 26, 2025
  • Report date: February 4, 2026
  • Hazard classification: Class II
  • Affected product UPC: 048155920200

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 Classification

Product TypePregnancy Test
Sold At
Multiple Retailers

Product Details

Model Numbers
UPC 048155920200
Affected States
ALL
Report Date
February 4, 2026
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.

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CGMP Deviations:
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