IBSA Pharma recalls TIROS: levothyroxine oral solution with subpotent drug risk. Affected units have NDC 71858-0110-5, lot 220856, expiring 2/2024. No remedy specified in recall notice.
Subpotent Drug
IBSA Pharma is recalling 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, 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 specific lot number (220856) of the oral solution. Those with thyroid conditions are most at risk.
Check for the product name 'TIROSINT - SOL' with 25 microgram/mL concentration. The lot number 220856 and expiration date 2/2024 are specific identifiers for this recall.
Look for the lot number 220856 and expiration date 2/2024 on the packaging.
The recall states it may be subpotent, meaning it could have less active ingredient than labeled. However, the official notice does not specify if taking it causes harm.
Check the lot number 220856 and expiration date 2/2024 on the packaging. The product name is TIROSINT - SOL (levothyroxine sodium) Oral Solution.
The recall notice does not specify a remedy, so no action is required beyond checking the product details.
We’ve drafted a message you can send IBSA Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0335-2023 — IBSA Pharma IBSA Pharma Hello, I own a IBSA Pharma that is covered by recall D-0335-2023 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.
