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Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 70,959 testosterone pellets on January 26, 2026, due to potential metal contamination. Consumers must stop using the product immediately. The recall affects multiple lots distributed nationwide in the USA.

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#: 251000122, Exp. 04/01/2026, 251000151, Exp. 08/02/2026, 251000155, Exp. 08/08/2026, 251000173, Exp. 09/05/2026.
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 to treat low testosterone levels in men. They provide a steady release of testosterone into the bloodstream over time.

Why This Is Dangerous

The potential presence of metal particulate matter in testosterone pellets can lead to serious health risks, including inflammation or damage to internal organs.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face health risks from using contaminated products, and they should take immediate action to stop use and seek guidance.

Practical Guidance

How to identify if yours is affected

  1. Check the packaging for the lot number and expiration date.
  2. Compare your lot number against the recalled lots listed in the recall notice.
  3. If in doubt, consult your healthcare provider.

Where to find product info

Lot numbers and expiration dates are typically printed on the product packaging or label.

What timeline to expect

Refund processing typically takes 4-6 weeks after the returned product is received.

If the manufacturer is unresponsive

  • Follow up with F.H. INVESTMENTS, Inc. via phone or email.
  • Document all correspondence and attempts to resolve the issue.

How to prevent similar issues

  • Always check recall notices for medications before use.
  • Consult with healthcare providers before starting any new medication.

Documentation advice

Keep records of your purchase, including receipts and any correspondence regarding the recall.

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Product Details

The recall involves Testosterone, 50.0 mg, 1 Sterile Pellet by Asteria Health. Affected lot numbers include 251000122, 251000151, 251000155, and 251000173 with expiration dates ranging from April 1, 2026, to September 5, 2026. The pellets were distributed nationwide.

Key Facts

  • Recall date: January 26, 2026
  • Quantity recalled: 70,959 pellets
  • Potential metal contamination
  • Nationwide distribution in the USA

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#: 251000122
Exp. 04/01/2026
251000151
Exp. 08/02/2026
251000155
+3 more
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

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