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
- Estradiol Pellet
- Model numbers
- Lot#: 253000126, Exp. 06/09/2026.
- 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
Estradiol pellets are a form of hormone replacement therapy commonly used to treat menopausal symptoms and hormone deficiencies. These pellets are inserted subcutaneously to provide a steady release of estradiol into the bloodstream.
Why This Is Dangerous
The hazard arises from the potential presence of metal particles in the estradiol pellets, which could lead to serious health issues if ingested or absorbed. Contaminated products can cause adverse reactions, including inflammation and other health complications.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall creates an urgent need for affected consumers to cease usage immediately. This can lead to inconvenience as they must seek alternative treatments while ensuring their safety.
Practical Guidance
How to identify if yours is affected
- Check the lot number on your estradiol pellets packaging.
- Confirm if the lot number is 253000126 to determine if your product is affected.
- Look for the expiration date, which should be June 9, 2026.
Where to find product info
The lot number and expiration date can typically be found on the packaging or label of the estradiol pellets.
What timeline to expect
Expect refund processing to take approximately 4-6 weeks after the manufacturer receives the returned product.
If the manufacturer is unresponsive
- Document all correspondence with the manufacturer or healthcare provider.
- Follow up via phone or email if you do not receive a timely response.
- Consider reporting the issue to the FDA if no resolution is reached.
How to prevent similar issues
- Always check for recalls before using medications or health products.
- Consult your healthcare provider regarding any concerns about product safety.
- Look for certifications and safety tests when purchasing health-related products.
Documentation advice
Keep records of all communications regarding the recall, including emails and letters. Retain any receipts or proof of purchase as they may be required for refunds.
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Product Details
The recall involves 133 estradiol pellets manufactured by Asteria Health. The affected lot number is 253000126, expiring on June 9, 2026. The product was distributed nationwide in the United States.
Key Facts
- Recall date: January 26, 2026
- Quantity recalled: 133 pellets
- Affected lot number: 253000126
- Expiration date: June 9, 2026
- Classification: Class II
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Safety Guide
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