HIGH

Asteria Health Recalls Estradiol Pellets Over Metal Contamination

Asteria Health recalled 1,699 sterile estradiol pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately and contact their healthcare provider for advice. The recall affects pellets distributed nationwide in the USA.

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 recall includes estradiol pellets, 18 mg, Lot#: 253000123, with an expiration date of June 2, 2026. The product is distributed by Asteria Health, located at 432 Industrial Ln, Birmingham, AL 3521.

The Hazard

The estradiol pellets may contain foreign substances, specifically potential metal particulate matter. This poses a significant health risk as these particles can cause serious injury.

Reported Incidents

No specific incidents or injuries have been reported at this time. The presence of metal particles raises concerns about potential harm to consumers.

What to Do

Consumers should immediately stop using the estradiol pellets. Contact F.H. Investments, Inc. or your healthcare provider for guidance on next steps.

Contact Information

For more information, consumers can visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0311-2026 or reach out directly to Asteria Health.

Key Facts

  • Recall Date: January 26, 2026
  • Distribution: Nationwide in the USA
  • Quantity Recalled: 1,699 pellets
  • Hazard: Potential metal particulate contamination
  • Classification: Class II

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
Lot#: 253000123
Exp. 06/02/2026.
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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