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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 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#: 256000105, Exp. 09/19/2026.
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 26, 2026
Reported by FDA DRUG
February 18, 2026
RecallRadar source check
February 25, 2026
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
The product is a testosterone pellet used for hormone replacement therapy. Consumers buy it to manage low testosterone levels and related health issues.
Why This Is Dangerous
The contamination risk arises from the potential presence of metal particles, which can cause serious health complications if ingested.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the product immediately, which may interrupt their hormone therapy regimen. This could lead to health implications if alternative therapies are not arranged promptly.
Practical Guidance
How to identify if yours is affected
- Check the lot number on the packaging.
- Ensure it matches Lot#: 256000105.
- Verify the expiration date to confirm the product is affected.
Where to find product info
Look for the lot number and expiration date on the product packaging, usually found on the label or bottom of the box.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks after contacting the manufacturer.
If the manufacturer is unresponsive
- Document all correspondence with the manufacturer.
- Follow up via phone or email if no response is received.
- Consider filing a complaint with the FDA.
How to prevent similar issues
- Always check for recalls before purchasing medications.
- Consult healthcare providers for alternative products when recalls occur.
- Be aware of product expiration dates and lot numbers.
Documentation advice
Keep records of your purchase, any correspondence regarding the recall, and document the lot number and expiration date.
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Product Details
The recall involves testosterone pellets containing 200mg of testosterone and 40mcg of triamcinolone acetonide. The affected lot number is 256000105, expiring on September 19, 2026. The product is manufactured by F.H. INVESTMENTS, Inc. and was sold nationwide.
Key Facts
- Recall date: January 26, 2026
- Reported date: February 18, 2026
- Quantity recalled: 7,840 pellets
- Potential health risk: High
- Manufacturer: F.H. INVESTMENTS, Inc.
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Safety Guide
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