Quick Facts at a Glance
- Recall Date
- January 16, 2026
- Hazard Level
- HIGH
- Brand
- Specialty Process Labs
- 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
- Specialty Process Labs
- Product type
- Thyroid Medication
- Model numbers
- Lot #H22254-1XV, Exp. 01/31/2027
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 16, 2026
Reported by FDA DRUG
January 28, 2026
RecallRadar source check
February 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Subpotent Drug
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Specialty Process Labs LLC or your healthcare provider for guidance. Notification method: Letter
About This Product
Thyroid medications like Thyroid, USP are commonly used to treat hypothyroidism and other thyroid disorders. Patients rely on these medications to manage their thyroid hormone levels effectively.
Why This Is Dangerous
The product is classified as subpotent, meaning it does not contain the required strength to be effective for treatment. This can lead to insufficient hormone levels in patients who depend on it for their health.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients using this recalled medication may experience inadequate treatment, leading to potential health risks. Immediate action is necessary to switch to a safe alternative.
Practical Guidance
How to identify if yours is affected
- Check the lot number on your medication packaging.
- Verify the expiration date for your product.
- Refer to the FDA recall notice for additional details.
Where to find product info
Lot numbers and expiration dates are usually printed on the product label or packaging.
What timeline to expect
Refund processing or replacement timelines may vary; expect approximately 4-6 weeks for resolution.
If the manufacturer is unresponsive
- Document your communication attempts with Specialty Process Labs.
- Consider contacting the FDA for assistance if the company does not respond.
How to prevent similar issues
- Always check recall notices for medications regularly.
- Consult with your healthcare provider about medication changes or alternatives.
Documentation advice
Keep records of your purchase, including receipts, and any correspondence with the manufacturer.
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Product Details
The recall involves Thyroid, USP, Rx only, Net Wt: 0.50kg. The affected lot number is H22254-1XV, with an expiration date of January 31, 2027. The product was distributed nationwide.
Key Facts
- Recall date: January 16, 2026
- Report date: January 28, 2026
- Classification: Class II
- Quantity recalled: 58 grams
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Safety Guide
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