Mylan recalls 150 mcg levothyroxine tablets due to potential super-potent drug potency. This may cause unsafe medication levels. Check NDC 51079-445-20 and lot 3116074 for affected units.
Super-Potent Drug: Out of specification potency results were obtained.
Mylan is recalling 150 mcg levothyroxine tablets that may be too potent. This could lead to unsafe medication levels if taken as directed. Affected units have specific NDC and lot numbers.
The tablets may have higher-than-stated potency, leading to potentially unsafe medication levels. This could cause adverse effects if taken without medical supervision.
People with prescriptions for this medication are affected. Those taking the recalled product may face unsafe medication levels.
Check for NDC 51079-445-20 and lot number 3116074 on the blister pack. The product was made in India and expires September 30, 2025.
Look for NDC 51079-445-20 and lot number 3116074 on the blister pack.
The recall states the product may have super-potent drug potency, but the official notice does not specify if it's safe to use.
The recall does not provide a remedy, so the official notice does not specify actions to take.
Check for NDC 51079-445-20 and lot number 3116074 on the blister pack. The product was made in India and expires September 30, 2025.
We’ve drafted a message you can send Mylan to request your refund or repair — edit it as you like.
Subject: Recall D-0290-2025 — Mylan Mylan Hello, I own a Mylan that is covered by recall D-0290-2025 from Mylan. 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.
