HIGH

Asteria Health Recalls Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 1,758 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects pellets distributed nationwide in the USA. Consumers should stop using the product immediately and contact their healthcare providers for guidance.

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 involves Testosterone, 62.5 mg, 1 Sterile Pellet, Lot#: 251000125, Exp. 06/02/2026. The product is distributed by Asteria Health, located at 432 Industrial Ln, Birmingham, AL 35211.

The Hazard

The recall stems from the potential presence of metal particulate matter in the testosterone pellets. This contamination poses a serious health risk to users.

Reported Incidents

There have been no reported injuries or incidents related to this recall at this time. However, the risk of contamination warrants immediate action.

What to Do

Stop using the testosterone pellets immediately. Consumers should contact F.H. INVESTMENTS, Inc. (dba Asteria Health) or their healthcare provider for guidance on the next steps.

Contact Information

For more information, consumers can reach Asteria Health at the contact details provided in the recall notification letter.

Key Facts

  • 1,758 pellets recalled
  • Potential metal contamination
  • Distributed nationwide in the USA
  • Stop use immediately
  • Contact healthcare provider for guidance

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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#: 251000125
Exp. 06/02/2026.
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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