HIGH

Asteria Health Recalls Estradiol Pellets Due to Metal Contamination

Asteria Health recalled 1,475 estradiol pellets on January 26, 2026, due to potential metal particulate contamination. This recall affects products distributed nationwide in the United States. Consumers should stop using the product immediately and seek guidance from their healthcare provider.

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 for hormone replacement therapy, primarily in women undergoing menopause. They help alleviate symptoms such as hot flashes and mood swings.

Why This Is Dangerous

The presence of metal particulate matter in the pellets can lead to serious health risks if ingested, including potential toxicity and adverse reactions.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall signifies a potential health risk for consumers relying on this medication, necessitating immediate action to prevent possible health complications.

Practical Guidance

How to identify if yours is affected

  1. Check the lot number on your estradiol pellets packaging.
  2. Verify the expiration date to ensure it matches the recalled batch.
  3. If you find a match, stop using the product immediately.

Where to find product info

Lot numbers and expiration dates can typically be found on the product packaging or accompanying documentation.

What timeline to expect

Expect a response regarding refunds or replacements within 4-6 weeks after contacting the manufacturer.

If the manufacturer is unresponsive

  • Follow up with the manufacturer through multiple channels (email, phone).
  • Consider filing a complaint with the FDA if there is no response.

How to prevent similar issues

  • Always check for recalls on medications before use.
  • Consult your healthcare provider about alternatives if a recall occurs.

Documentation advice

Keep all receipts, communication with the manufacturer, and any medical records related to the use of the recalled product.

Product Details

The recalled product is Estradiol, 20 mg, 1 Sterile Pellet, with lot number 253000124 and an expiration date of June 2, 2026. It was distributed nationwide in the USA. There are no price details available.

Key Facts

  • Recall Date: January 26, 2026
  • Quantity Recalled: 1,475 pellets
  • Hazard: Presence of metal particulate
  • Classification: Class II
  • Distribution: Nationwide in the USA

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#: 253000124
Exp. 06/02/2026.
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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