HIGH

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 89,074 testosterone pellets on January 26, 2026. The recall stems from potential metal particulate contamination. Consumers must stop using the product and contact their healthcare provider immediately.

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 Testosterone, 25.0 mg, 1 Sterile Pellet, with NDC: 79559-1025-32. It is part of multiple lots, including Lot#: 251000130, 251000137, 251000152, 251000168, and 251000170, with varying expiration dates from June 2, 2026, to September 3, 2026.

The Hazard

The recall is due to the potential presence of metal particulate matter in the testosterone pellets. This contamination poses a serious health risk to consumers, as it could lead to severe adverse health effects.

Reported Incidents

As of now, there have been no reported injuries or incidents related to this recall. However, the presence of foreign substances in medications is considered a high-risk issue.

What to Do

Consumers and healthcare providers should stop using this product immediately. They should contact F.H. INVESTMENTS, Inc. (dba Asteria Health) for guidance and further information.

Contact Information

For more information, contact F.H. INVESTMENTS, Inc. at their Birmingham, AL address or visit their website for updates regarding the recall.

Key Facts

  • 89,074 testosterone pellets recalled
  • Potential metal contamination risk
  • Stop using product immediately
  • Contact healthcare provider for guidance
  • Recalled product includes several lots

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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#: 251000130
251000137
251000152
251000168
251000170
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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