West-Ward recalls 2.5 mg methotrexate tablets with unsmooth surfaces and illegible labels. These tablets may not be properly identified or scored, posing risks for patients using prescription medication.
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
West-Ward is recalling methotrexate tablets that have unsmooth surfaces and two tablets with illegible identification and scoring. This could lead to incorrect dosing or medication confusion for patients using these prescription drugs.
The tablets have an unsmooth surface and two tablets show illegible identification and scoring. This could cause confusion about the medication's identity or dosage, potentially leading to incorrect use.
Patients prescribed methotrexate by a doctor who own or use the recalled tablets. Those with specific lot numbers and expiration dates are most at risk.
Check for the lot numbers AB7486B (exp Dec 2023), AB8766B (exp April 2024), or AB9484B (exp Aug 2024) on the packaging. The product is a 2.5 mg methotrexate tablet, 10x10 unit-dose per carton, prescribed only.
Look for lot numbers AB7486B (exp Dec 2023), AB8766B (exp April 2024), or AB9484B (exp Aug 2024) on the packaging.
The tablets have an unsmooth surface and two tablets demonstrate illegible identification and scoring.
Lot AB7486B (exp Dec 2023), Lot AB8766B (exp April 2024), and Lot AB9484B (exp Aug 2024).
Check for the lot numbers AB7486B, AB8766B, or AB9484B on the packaging, which are associated with the 2.5 mg methotrexate tablets.
We’ve drafted a message you can send West-Ward to request your refund or repair — edit it as you like.
Subject: Recall D-0066-2024 — West-Ward West-Ward Hello, I own a West-Ward that is covered by recall D-0066-2024 from West-Ward. 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.
