HIGH

Asteria Health Recalls Testosterone Pellets Over Metal Contamination Risk

Asteria Health recalled 1,015 testosterone pellets on January 26, 2026 due to potential metal particulate contamination. The recall affects products distributed nationwide in the United States. Consumers must stop using the pellets immediately and contact their healthcare provider 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 recalled product is Testosterone, 303 mg, 1 Sterile Pellet, manufactured by F.H. INVESTMENTS, Inc. The affected lot number is 251000124 with an expiration date of June 2, 2026.

The Hazard

The recall stems from the potential presence of metal particulate matter in the testosterone pellets. This contamination poses serious health risks if ingested.

Reported Incidents

As of now, there are no reported injuries or incidents associated with the contamination. However, the risk of serious health consequences remains high.

What to Do

Consumers should stop using the testosterone pellets immediately. Contact F.H. INVESTMENTS, Inc. or your healthcare provider for further guidance and possible refund options.

Contact Information

For more information, call F.H. INVESTMENTS, Inc. at the contact number provided on the recall notice. Additional details can be found on the FDA website.

Key Facts

  • Recall date: January 26, 2026
  • Quantity recalled: 1,015 pellets
  • Lot number: 251000124
  • Expiration date: June 2, 2026
  • Nationwide distribution in the USA

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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#: 251000124
Exp. 06/02/2026.
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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