RemedyRepack Inc. recalls Simvastatin 40mg tablets due to cGMP deviations in manufacturing. Affected lots have specific expiration dates and NDC codes. Consumers should check their bottles for the listed lot numbers and expiration dates.
cGMP Deviations
RemedyRepack Inc. is recalling Simvastatin 40mg tablets from specific lots because of manufacturing deviations. This recall affects people who have these particular bottle sizes and lot numbers, which may pose a risk to safety.
The recall is due to cGMP deviations, which are manufacturing quality control issues that could affect the safety and effectiveness of the medication. However, the specific risk to consumers is not clearly described in the recall notice.
People who have the 30-count or 90-count Simvastatin 40mg tablets with the listed lot numbers and expiration dates are affected. Those taking this medication for cholesterol management are most at risk.
Check your Simvastatin 40mg tablets for the following lot numbers: J0656821-103122 (exp. 11/30/2023), J0638547-080922 (exp. 08/31/2023), J0633575-071822 (exp. 07/31/2023) for 30-count bottles, and B1965081-111622 (exp. 03/31/2025) among others for 90-count bottles.
Look for the specific lot numbers and expiration dates listed in the recall notice on your Simvastatin 40mg tablets.
The recall is due to cGMP deviations in manufacturing, which are quality control issues that could affect the safety and effectiveness of the medication.
Check your bottles for the listed lot numbers and expiration dates. If you have the affected lots, stop using them and contact your doctor.
Yes, the affected lots have specific expiration dates like 11/30/2023, 08/31/2023, and 03/31/2025.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0503-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0503-2023 from RemedyRepack. 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.
