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
- Hormonal Pellet
- Model numbers
- Lot#: 253000132, Exp. 06/16/2026, 253000139, 253000140, Exp. 07/21/2026, 253000150, Exp. 08/08/2026, 253000151 +4 more
- 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
Estradiol pellets are used for hormone replacement therapy in individuals undergoing menopause or hormonal imbalances. They provide a steady release of hormones into the body and are favored for their convenience and effectiveness.
Why This Is Dangerous
The recall is due to the potential presence of metal particulate matter, which can contaminate the pellets. Ingesting these particles poses health risks that can lead to serious complications.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the affected Estradiol pellets immediately to avoid potential health risks. This could cause inconvenience as users may need to seek alternative hormone replacement therapies.
Practical Guidance
How to identify if yours is affected
- Check the lot numbers of your Estradiol pellets against the recalled list.
- Verify the expiration dates to ensure they fall within the affected range.
- Contact your healthcare provider if you have concerns about your product.
Where to find product info
Lot numbers and expiration dates can typically be found on the packaging of the pellets or on the label of the product container.
What timeline to expect
Expect a timeline of 4-6 weeks for refund processing after returning the product.
If the manufacturer is unresponsive
- Contact the FDA for guidance on how to escalate your complaint.
- Document all correspondence with the company regarding the recall.
How to prevent similar issues
- When purchasing hormone replacement products, look for certifications and quality assurances.
- Consult with a healthcare provider about the safety of products before use.
- Stay informed about recalls and safety alerts related to health products.
Documentation advice
Keep records of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.
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Product Details
The recalled product is Estradiol, 10 mg, sold in sterile pellet form. The lot numbers affected include 253000132, 253000139, 253000140, 253000150, 253000151, 253000161, and 253000162. The expiration dates range from June 16, 2026, to September 12, 2026.
Key Facts
- Recall date: January 26, 2026
- Nationwide distribution in the USA
- Potential contamination with metal particles
- Class II recall
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Safety Guide
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