IBSA Pharma recalls TIROSINT levothyroxine oral solution (44 mcg/mL) with subpotent drug risk. Affected units have specific NDC and lot numbers. Consumers should contact pharmacy for guidance.
Subpotent Drug
IBSA Pharma has recalled TIROSINT levothyroxine oral solution because it may not contain the correct amount of active ingredient. This could lead to improper thyroid hormone levels if used without medical supervision.
The medication may have less active levothyroxine than labeled, which could result in insufficient thyroid hormone levels. This might cause symptoms like fatigue, weight gain, or depression if not properly managed by a healthcare provider.
People prescribed this medication by a doctor who received the recalled product. Those with thyroid conditions are most at risk if they use it without medical guidance.
Check the product label for 'TIROSINT - SOL (levothyroxine sodium) Oral Solution, 44 microgram/mL'. Look for NDC 71858-0113-5 and lot numbers 220553 (expiring 11/2023) or 221056 (expiring 04/2024).
Look for the NDC code 71858-0113-5 and lot numbers 220553 or 221056 on the packaging.
Reach out to your pharmacy for guidance on whether the product is affected and how to proceed.
The recall is due to a potential subpotent drug risk, meaning it may not contain the correct amount of active ingredient. It is not safe to use without medical supervision.
Check the product label for the NDC code and lot numbers. Contact your pharmacy for guidance on next steps.
Look for the NDC 71858-0113-5 and lot numbers 220553 (expiring 11/2023) or 221056 (expiring 04/2024) on the packaging.
We’ve drafted a message you can send IBSA Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0337-2023 — IBSA Pharma IBSA Pharma Hello, I own a IBSA Pharma that is covered by recall D-0337-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
