Quick Facts at a Glance
- Recall Date
- January 26, 2026
- Hazard Level
- HIGH
- Brand
- F.H. INVESTMENTS, Inc.
- Category
- Health & Personal Care
- Sold At
- Unknown
- 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#: 256000104, Exp. 07/30/2026. .
- Sold at
- Unknown
- 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
Testosterone pellets are used in hormone replacement therapy for individuals with low testosterone levels. Consumers purchase these products to manage symptoms related to testosterone deficiency.
Why This Is Dangerous
The recall is due to the potential contamination of pellets with metal particulate matter, which can pose serious health risks if administered.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers who have used these pellets should be aware of possible health risks and seek medical advice. The recall may also cause inconvenience for those relying on this treatment.
Practical Guidance
How to identify if yours is affected
- Check your product's lot number against the recalled lot number: 256000104.
- Verify the expiration date on the packaging; it should read July 30, 2026.
- If you have used the product, monitor for any adverse symptoms and consult your healthcare provider.
Where to find product info
Lot numbers and expiration dates are typically found on the packaging or label of the product.
What timeline to expect
Expect a timeline of 4-6 weeks for processing refunds or replacements.
If the manufacturer is unresponsive
- Contact the manufacturer directly for follow-up.
- Consider reaching out to the FDA for further assistance.
How to prevent similar issues
- Inquire about product testing and safety certifications before purchasing.
- Consult healthcare providers about the safety of medications being prescribed.
- Stay informed on recalls and safety alerts through government websites.
Documentation advice
Keep a record of your purchase, any symptoms experienced, and correspondence with medical professionals.
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Product Details
The recall involves Testosterone 100mg and Triamcinolone Acetonide 20mcg sterile pellets, lot number 256000104, with an expiration date of July 30, 2026. The product was distributed nationwide in the USA.
Key Facts
- Recall Date: January 26, 2026
- Reported by: F.H. Investments, Inc.
- Risk Level: High
- Quantity Recalled: 4,599 pellets
- Distribution: Nationwide in the USA
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Safety Guide
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