West-Ward recalls 5mg methadone tablets with illegible unit-dose labels. This could cause medication errors if misidentified. Contact your pharmacy for assistance.
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
West-Ward is recalling 5mg methadone hydrochloride tablets that have illegible product labels. This risk could lead to medication errors if someone mistakenly identifies the tablets.
The tablets have illegible product identification, which could cause confusion if someone tries to identify the medication. This might lead to incorrect dosing or medication errors.
Prescription patients using the recalled methadone tablets. Those with the specific lot number AC2556A are most at risk.
Check for the lot number AC2556A on the packaging. The product is a 5mg methadone hydrochloride tablet with 10x10 unit-dose configuration.
Look for the lot number AC2556A on the packaging to confirm if it's recalled.
The recall is for illegible labels, not safety issues. If you have the specific lot number, contact your pharmacy for guidance.
Check for the lot number AC2556A on the packaging. The product is a 5mg methadone hydrochloride tablet with 10x10 unit-dose configuration.
The recall does not specify a remedy. Check with your pharmacy for advice on next steps.
We’ve drafted a message you can send West-Ward to request your refund or repair — edit it as you like.
Subject: Recall D-0183-2025 — West-Ward West-Ward Hello, I own a West-Ward that is covered by recall D-0183-2025 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.
