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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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.

The Hazard

The recall addresses the potential presence of metal particulate matter in the estradiol pellets. This contamination poses serious health risks to users, particularly if ingested.

Reported Incidents

No specific incidents or injuries have been reported at this time. However, given the potential for serious health implications, the hazard is classified as high.

What to Do

Stop using the product immediately. Contact F.H. Investments, Inc. or your healthcare provider for further guidance. Notifications will be sent via letter.

Contact Information

For more information, contact F.H. Investments, Inc. at their Birmingham, Alabama location or visit their website.

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

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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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