IBSA Pharma recalls TIROSINT levothyroxine oral solution (37.5 mcg/mL) with subpotent drug risk. This affects specific lots manufactured in Switzerland. Contact for return instructions.
Subpotent Drug
IBSA Pharma is recalling a specific levothyroxine oral solution product due to a subpotent drug issue. This means the medication may not contain enough active ingredient to be effective. Patients should not use this product without consulting their doctor.
The medication contains less active levothyroxine than intended, which could lead to ineffective treatment of thyroid conditions. This is a subpotent drug issue, meaning the product may not work as prescribed.
People prescribed this specific levothyroxine oral solution by a doctor. Those with thyroid conditions are most at risk if they use the recalled product.
Check for the product name 'TIROSINT - SOL (levothyroxine sodium) Oral Solution, 37.5 microgram/mL'. Look for the lot numbers 220552 (expiring 11/2023) or 221055 (expiring 04/2024).
Verify the lot number and expiration date on the product label to confirm if it's in the recalled range.
Talk to your healthcare provider about alternative treatment options if you have the recalled product.
The product has a subpotent drug issue, meaning it may not contain enough active ingredient. Do not use without consulting your doctor.
Check for the lot numbers 220552 (expiring 11/2023) or 221055 (expiring 04/2024) on the product label.
Contact your doctor for alternative treatment options. Do not use the product without medical advice.
We’ve drafted a message you can send IBSA Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0336-2023 — IBSA Pharma IBSA Pharma Hello, I own a IBSA Pharma that is covered by recall D-0336-2023 from IBSA Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
