IBSA Pharma recalls TIROSINT levothyroxine oral solution (137 mcg/mL) with subpotent drug risk. Affected units have specific NDC and lot numbers. Consumers should contact pharmacy for guidance.
Subpotent Drug
IBSA Pharma is recalling TIROSINT levothyroxine oral solution because it may contain less active drug than labeled. This could lead to improper thyroid hormone levels if used without medical supervision.
The medication may have lower than labeled active ingredient (subpotent), which could result in insufficient thyroid hormone levels. This might cause symptoms like fatigue, weight gain, or depression if not managed by a healthcare provider.
People prescribed TIROSINT levothyroxine oral solution by a doctor. Those with thyroid conditions are most at risk if the medication is not properly dosed.
Check for the product name 'TIROSINT - SOL (levothyroxine sodium) Oral Solution', 137 microgram/mL concentration, and NDC 71858-0145-5. Lot numbers 220415 (expiring 10/2023) or 221052 (expiring 04/2024) are affected.
Your healthcare provider can advise on whether the medication is safe to use or needs replacement.
The recall is for a potential subpotent drug, meaning it may have less active ingredient than labeled. It is not immediately dangerous but could affect thyroid hormone levels if used without medical supervision.
Check the product label for NDC 71858-0145-5 and lot numbers 220415 (expiring 10/2023) or 221052 (expiring 04/2024).
The recall does not require immediate discontinuation. Contact your pharmacist for guidance on whether to continue using the medication.
We’ve drafted a message you can send IBSA Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0343-2023 — IBSA Pharma IBSA Pharma Hello, I own a IBSA Pharma that is covered by recall D-0343-2023 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.
