HIGH

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 194,336 testosterone pellets on January 26, 2026 due to potential metal contamination. Consumers must stop using the product immediately and contact their healthcare providers. The recall affects nationwide distribution in the USA.

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, 200 mg, 1 Sterile Pellet from Asteria Health. Lot numbers include 251000127, 251000128, 251000133, and several others with expiration dates ranging from June 3, 2026 to August 8, 2026. The product was distributed nationwide.

The Hazard

The recall stems from the potential presence of metal particulate matter in the pellets. This poses a high risk of serious injury to consumers who may use the contaminated product.

Reported Incidents

There are no reported injuries or incidents associated with the use of the contaminated testosterone pellets at this time.

What to Do

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

Contact Information

For questions, consumers can reach F.H. Investments, Inc. at the contact information provided in the recall notification letter.

Key Facts

  • 194,336 testosterone pellets recalled
  • Potential metal contamination hazard
  • Nationwide distribution in the USA
  • Stop using the product immediately

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
Lot#: 251000127
Exp. 06/03/2026
251000128
Exp. 06/05/2026
251000133
+15 more
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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