HIGH

Asteria Health Recalled Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 3,871 testosterone pellets on January 26, 2026, due to potential metal particulate matter. The recall affects products distributed nationwide in the USA. Consumers should stop using the product immediately and seek guidance from their 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 recall involves Testosterone, 12.5 mg, 1 Sterile Pellet, from Asteria Health. Lot numbers affected include 251000143 and 251000160, with expiration dates of July 7, 2026, and August 16, 2026, respectively. The product was distributed nationwide.

The Hazard

The recall is due to the potential presence of metal particulate matter in the testosterone pellets. This contamination could pose serious health risks to consumers.

Reported Incidents

No specific injuries or incidents have been reported in connection with this recall. The company has classified the recall as Class II, indicating a potential risk of serious health issues.

What to Do

Consumers should stop using the recalled testosterone pellets immediately. Contact F.H. INVESTMENTS, Inc. or your healthcare provider for guidance and information on returns.

Contact Information

For further details, call F.H. INVESTMENTS, Inc. at their customer service line or visit their website. Additional information is available on the FDA recall page.

Key Facts

  • Recalled product: Testosterone, 12.5 mg, 1 Sterile Pellet
  • Recall date: January 26, 2026
  • Total units recalled: 3,871
  • Potential hazard due to metal particulate matter
  • Immediate action required from consumers

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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#: 251000143
Exp. 07/07/2026
251000160
Exp. 08/16/2026
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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