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.
Subpotent Drug
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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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.
The recalled thyroid medication is subpotent, meaning it may not provide the expected therapeutic effects. This poses a significant health risk for patients relying on the medication for thyroid function.
No specific incidents of injury or adverse effects have been reported related to the recalled product.
Stop using the recalled medication immediately. Contact Specialty Process Labs LLC or your healthcare provider for further guidance on alternative treatments.
For more information, consumers can visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0294-2026.
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