HIGH

Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 14,848 estradiol pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The recall is classified as Class II, indicating a high hazard level.

Quick Facts at a Glance

Recall Date
January 26, 2026
Hazard Level
HIGH
Brand
F.H. INVESTMENTS, Inc.
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Presence of Foreign substance - potential presence of metal particulate matter

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact F.H. INVESTMENTS, Inc. (dba Asteria Health) or your healthcare provider for guidance. Notification method: Letter

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About This Product

Estradiol pellets are used in hormone replacement therapy for treating symptoms of menopause and other hormonal imbalances. They provide a controlled release of estrogen into the body to alleviate symptoms.

Why This Is Dangerous

The hazard arises from the potential presence of metal particulate matter within the estradiol pellets. Ingesting such contaminants can lead to severe health complications.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face health risks from using the affected estradiol pellets. The urgency to stop use and seek guidance adds to the inconvenience of managing hormonal therapy.

Practical Guidance

How to identify if yours is affected

  1. Check the packaging for the NDC number: 79559-3015-32.
  2. Verify the lot numbers: 253000118, 253000145, 253000146, 253000167.
  3. Confirm the expiration dates listed on the product.

Where to find product info

You can find the NDC number, lot numbers, and expiration dates on the product packaging or prescription label.

What timeline to expect

Expect a refund processing timeline of approximately 4-6 weeks after contacting the manufacturer.

If the manufacturer is unresponsive

  • Document all communication attempts with the company.
  • Consider contacting the FDA for additional guidance.
  • Keep records of your purchase and any correspondence.

How to prevent similar issues

  • Always check for recalls of medications before use.
  • Consult with a healthcare provider for alternative treatments if recalls occur.
  • Be aware of the signs of contamination in pharmaceutical products.

Documentation advice

Keep a copy of your purchase receipt, any correspondence with the manufacturer, and photographs of the product as evidence.

Product Details

The recalled product is ESTRADIOL, 15 mg, 1 Sterile Pellet, with NDC: 79559-3015-32. It was distributed nationwide in the USA. The affected lot numbers include 253000118, 253000145, 253000146, and 253000167, with expiration dates ranging from June 30, 2026, to September 23, 2026.

Key Facts

  • Recall Date: January 26, 2026
  • Quantity Recalled: 14,848 pellets
  • NDC: 79559-3015-32
  • Hazard Level: High

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 Details

Model Numbers
Lot#: 253000118
Exp. 02/21/2026
253000145
Exp. 08/02/2026
253000146
+3 more
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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