HIGH

Asteria Health Recalls Testosterone Pellet Over Metal Contamination

Asteria Health recalled 100 sterile pellets of testosterone and anastrozole on January 26, 2026. The recall stems from potential metal particulate contamination. Consumers must stop using the product immediately and consult 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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
F.H. INVESTMENTS, Inc.
Product type
Testosterone and Anastrozole Pellet
Model numbers
Lot#: 254000104, Exp. 05/27/2026
Sold at
Multiple Retailers
Where affected
ALL

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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About This Product

This product is a sterile pellet that combines testosterone and anastrozole, primarily used for hormone therapy. Consumers purchase it to manage conditions related to low testosterone levels.

Why This Is Dangerous

The hazard arises from the potential presence of metal particulate matter, which can pose serious health risks if ingested or injected. This contamination can lead to adverse health effects.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers affected by this recall face potential health risks and should cease use immediately. They may also experience inconvenience in managing their health conditions while seeking alternatives.

Practical Guidance

How to identify if yours is affected

  1. Check the lot number on your product.
  2. Verify the expiration date listed as May 27, 2026.
  3. Contact your healthcare provider if unsure about product safety.

Where to find product info

The lot number and expiration date can usually be found on the product packaging or label.

What timeline to expect

Expect a refund processing timeline of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Keep a record of all communications with the company.
  • Consider escalating your complaint to the FDA if no response is received.

How to prevent similar issues

  • Look for products with clear safety certifications.
  • Check for any reported recalls before purchase.
  • Consult healthcare providers for trusted brands.

Documentation advice

Document all correspondence with the manufacturer and keep copies of any receipts or notifications related to the recall.

Product Details

The recall affects testosterone 100mg and anastrozole 4mg sterile pellets, NDC: 79559-4104-01. These products were distributed nationwide in the USA. The lot number for the affected products is 254000104, with an expiration date of May 27, 2026.

Key Facts

  • Recall date: January 26, 2026
  • Hazard: Potential metal contamination
  • Consumers should stop using immediately

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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#: 254000104
Exp. 05/27/2026
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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