Accord Healthcare recalls 1000-count levothyroxine tablets due to subpotent drug levels. This may result in ineffective treatment. Check NDC 16729-451-17 and lot numbers for affected products.
Subpotent Drug: Assay below the approved specification
Accord Healthcare is recalling 1000-count levothyroxine tablets that may not contain enough active ingredient. This could lead to ineffective treatment for thyroid conditions. The recall is for prescription-only products with specific lot numbers.
The tablets may have less active drug than specified, leading to ineffective thyroid hormone levels. This could cause treatment failure for thyroid conditions but does not pose an immediate physical danger.
Prescription patients using the recalled levothyroxine tablets. Those with thyroid conditions are most at risk if the tablets are not effective.
Check for NDC 16729-451-17 and lot numbers D2300092 (exp 12/31/2025) or D2400722 (exp 03/31/2026). The product is a prescription-only 1000-count bottle of levothyroxine sodium tablets.
Verify the NDC code 16729-451-17 and lot numbers D2300092 or D2400722 on the bottle.
The tablets may contain less active drug than specified, which could lead to ineffective treatment for thyroid conditions.
Check for NDC 16729-451-17 and lot numbers D2300092 (exp 12/31/2025) or D2400722 (exp 03/31/2026).
The recall does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0521-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0521-2025 from Accord Healthcare. 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.
