IBSA Pharma recalls TIROSINT levothyroxine oral solution (100 mcg/mL) with subpotent drug risk. Affected units have specific NDC and lot numbers. Contact for remedy.
Subpotent Drug
IBSA Pharma recalled TIROSINT levothyroxine oral solution because it may not contain enough active ingredient. This could lead to improper thyroid hormone levels if used without medical supervision.
The medication may contain less active levothyroxine than labeled, potentially causing underactive thyroid function. This is a subpotent drug issue, not a safety hazard like breakage or fire.
People prescribed this medication by a doctor who received the recalled product. Those with thyroid conditions are most at risk.
Check for NDC 71858-0130-5 on the product label. The product was manufactured with lot numbers 220413 (expires 10/2023) or 220964 (expires 3/2024).
Look for NDC 71858-0130-5 and lot numbers 220413 or 220964 on the oral solution packaging.
The recall is for subpotent drug risk, meaning it may not contain enough active ingredient. It is not safe to use without medical supervision.
The official recall record does not specify a remedy, so contact your doctor or pharmacist for guidance.
Check for NDC 71858-0130-5 and lot numbers 220413 (expires 10/2023) or 220964 (expires 3/2024).
We’ve drafted a message you can send IBSA Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0332-2023 — IBSA Pharma IBSA Pharma Hello, I own a IBSA Pharma that is covered by recall D-0332-2023 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.
