Viatris recalls 500mg Valacyclovir tablets with possible missing 'M 122' imprint. This may affect identification and safety for prescription use.
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Viatris is recalling 500mg Valacyclovir tablets that might have a missing imprint 'M 122' on some tablets. This could make it harder to identify the correct medication, potentially leading to incorrect dosing.
The missing imprint 'M 122' could make it difficult to confirm the tablet's identity. This might lead to incorrect dosing if the patient or healthcare provider doesn't recognize the tablet as intended.
Prescription patients using Valacyclovir tablets from this specific batch. Those with the missing imprint may have difficulty verifying the correct medication.
Check for the imprint 'M 122' on the tablet. The product was manufactured for Mylan Pharmaceuticals in Morgantown, WV with specific lot numbers: 3183269 (expires May 2025) and 3157326 (expires June 2024).
Look for the 'M 122' imprint on the tablet. If missing, contact your pharmacy.
The recall is for potential missing 'M 122' imprint on some tablets, which could affect identification and safety.
Check for the 'M 122' imprint. If missing, contact your pharmacy for guidance.
The recall indicates a potential identification issue, not a direct risk of serious injury.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0481-2024 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0481-2024 from Viatris. 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.
