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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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
January 26, 2026
Status
ACTIVE
Severity
8/10

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 Pellet
Model numbers
Lot#: 251000125, Exp. 06/02/2026.
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 26, 2026

  2. Reported by FDA DRUG

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Testosterone pellets are used for hormone replacement therapy in men with low testosterone levels. They are often chosen for their ease of use and effectiveness in delivering hormones steadily over time.

Why This Is Dangerous

The recall is due to the potential presence of metal particulate matter in the testosterone pellets. Such contamination can pose serious health risks if ingested.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers face potential health risks from using the contaminated product. Immediate action is necessary to prevent adverse health effects.

Practical Guidance

How to identify if yours is affected

  1. Check the packaging for Lot#: 251000125.
  2. Verify the expiration date is 06/02/2026.
  3. If you have pellets from this lot, stop using them immediately.

Where to find product info

Look for the lot number and expiration date on the blister pack or box of testosterone pellets.

What timeline to expect

Expect a refund or replacement to be processed within 4-6 weeks after contacting Asteria Health.

If the manufacturer is unresponsive

  • Contact Asteria Health again to follow up.
  • Reach out to your healthcare provider for assistance.
  • File a complaint with the FDA if no response is received.

How to prevent similar issues

  • Always verify lot numbers before purchasing medications.
  • Research manufacturers for safety records and recalls.
  • Consult healthcare providers for alternative treatment options.

Documentation advice

Keep records of your purchase, any medical consultations, and any symptoms experienced after using the product.

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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.

Key Facts

  • Potential metal contamination
  • Distributed nationwide in the USA
  • Stop use immediately
  • Contact healthcare provider for guidance

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

Related Recalls

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F.H. INVESTMENTS, Inc.
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