Viatris recalls 330mg Lyrica CR extended-release tablets with failed dissolution specifications. Rx-only bottles distributed by Parke-Davis Division of Pfizer. No remedy specified in official notice.
Failed Dissolution Specifications
Viat:ris is recalling 330mg Lyrica CR extended-release tablets that failed dissolution tests. This means the medication may not release properly in the body, potentially affecting treatment effectiveness. The recall applies to specific lot numbers and expiration dates.
Failed dissolution specifications mean the tablets may not release the medication properly in the body. This could lead to inconsistent dosing and reduced effectiveness of the treatment. The hazard is not described as causing immediate harm but affects the drug's intended function.
Prescription owners of Lyrica CR 330mg tablets with specific lot numbers and expiration dates (August 2022) are affected. Patients using these tablets for nerve pain or other conditions are most at risk.
Check for Lyrica CR 330mg tablets in 30-count bottles with lot numbers DN5396, EP9726, or EK2417 and expiration date August 2022. These are prescription-only products distributed by Parke-Davis Division of Pfizer.
Identify if your Lyrica CR 330mg tablets have the specific lot numbers DN5396, EP9726, or EK2417 with an expiration date of August 2022.
The recall is for failed dissolution specifications, which may affect medication effectiveness but does not describe a risk of serious injury or death. The official notice does not specify a remedy.
The official recall notice does not specify a remedy, so no action is required beyond checking product details.
Check for lot numbers DN5396, EP9726, or EK2417 with an expiration date of August 2022 on the 330mg Lyrica CR tablets.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0851-2021 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0851-2021 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.
