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
- Hormone Replacement Pellet
- Model numbers
- Lot#: 253000124, Exp. 06/02/2026.
- 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 used for hormone replacement therapy, primarily in women undergoing menopause. They help alleviate symptoms such as hot flashes and mood swings.
Why This Is Dangerous
The presence of metal particulate matter in the pellets can lead to serious health risks if ingested, including potential toxicity and adverse reactions.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall signifies a potential health risk for consumers relying on this medication, necessitating immediate action to prevent possible health complications.
Practical Guidance
How to identify if yours is affected
- Check the lot number on your estradiol pellets packaging.
- Verify the expiration date to ensure it matches the recalled batch.
- If you find a match, stop using the product immediately.
Where to find product info
Lot numbers and expiration dates can typically be found on the product packaging or accompanying documentation.
What timeline to expect
Expect a response regarding refunds or replacements within 4-6 weeks after contacting the manufacturer.
If the manufacturer is unresponsive
- Follow up with the manufacturer through multiple channels (email, phone).
- Consider filing a complaint with the FDA if there is no response.
How to prevent similar issues
- Always check for recalls on medications before use.
- Consult your healthcare provider about alternatives if a recall occurs.
Documentation advice
Keep all receipts, communication with the manufacturer, and any medical records related to the use of the recalled product.
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Product Details
The recalled product is Estradiol, 20 mg, 1 Sterile Pellet, with lot number 253000124 and an expiration date of June 2, 2026. It was distributed nationwide in the USA. There are no price details available.
Key Facts
- Recall Date: January 26, 2026
- Quantity Recalled: 1,475 pellets
- Hazard: Presence of metal particulate
- Classification: Class II
- Distribution: Nationwide in the USA
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Safety Guide
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