HIGH

Specialty Process Labs Issues Recall for Subpotent Thyroid Drug

Specialty Process Labs recalled 58 grams of Thyroid, USP due to subpotency. The recall affects products distributed nationwide. Consumers should stop using the drug immediately and contact their healthcare provider.

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

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

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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

  1. Check the lot number on your medication packaging.
  2. Verify the expiration date for your product.
  3. 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.

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
  • Nationwide distribution

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot #H22254-1XV
Exp. 01/31/2027
Affected States
ALL
Report Date
January 28, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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