HIGH

Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 50,990 Estradiol pellets on January 26, 2026, due to potential metal particulate matter contamination. The recall affects products distributed nationwide in the USA. Consumers should stop using the pellets immediately and seek guidance from healthcare providers.

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, 6 mg, 1 Sterile Pellet. The affected lot numbers include 253000127, 253000133, 253000138, 253000141, 253000144, 253000147, 253000148, 253000149, 253000152, 253000153, and 253000156. The expiration dates range from June 9, 2026, to August 22, 2026.

The Hazard

The recall stems from the presence of a foreign substance, specifically potential metal particulate matter. This contamination poses a significant health risk to consumers who may use the affected pellets.

What to Do

Consumers and healthcare providers should stop using the product immediately. Contact F.H. Investments, Inc. for guidance on how to proceed.

Contact Information

For more information, consumers can visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0307-2026 or call F.H. Investments, Inc.

Key Facts

  • Recall date: January 26, 2026
  • Quantity recalled: 50,990 pellets
  • Affected lot numbers include: 253000127, 253000133, 253000138
  • Expiration dates range from June 9 to August 22, 2026

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#: 253000127
Exp. 06/09/2026
253000133
Exp. 06/17/2026
253000138
+15 more
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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