Endo recalls Everolimus 5mg tablets due to impurity IP-C failing specifications. Rx-only product with specific lot number. Contact for return instructions.
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Endo is recalling Everolimus 5mg tablets because they contain an impurity that doesn't meet safety standards. This is a prescription-only medication that could pose risks if taken.
The tablets failed impurity testing for a specific chemical (IP-C) that could affect safety. This impurity may not be safe for patients taking the medication as prescribed.
Prescription patients who received Everolimus 5mg tablets with lot number 550172301 from the manufacturer. Those using this medication for medical treatment are most at risk.
Check for Everolimus 5mg tablets in cartons with 28 tablets (4 blister strips of 7 tablets each). Look for lot number 550172301 and expiration date January 2026.
Identify the lot number and expiration date on the packaging to confirm if your tablets are affected.
The recall indicates the tablets failed impurity testing, so they are not safe for use. Do not take these tablets.
Contact Endo directly for instructions on returning the product.
Look for lot number 550172301 and expiration date January 2026 on the packaging.
We’ve drafted a message you can send Endo to request your refund or repair — edit it as you like.
Subject: Recall D-0026-2026 — Endo Endo Hello, I own a Endo that is covered by recall D-0026-2026 from Endo. 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.
