PD-Rx Pharmaceuticals recalls Simvastatin 40mg tablets due to manufacturing quality control issues. Affected lots from specific production dates and quantities. Consumers should contact the company for details.
CGMP deviations.
PD-Rx Pharmaceuticals is recalling Simvastatin 40mg tablets (Rx only) because of manufacturing quality control deviations. This means the product may not meet safety standards, though the recall does not specify immediate health risks.
The recall is due to CGMP (Current Good Manufacturing Practice) deviations, which are quality control issues in the manufacturing process. These deviations could potentially affect the product's safety and effectiveness, but the exact risk is not specified in the recall notice.
People who have the specific 30-count or 90-count bottles of Simvastatin 40mg with the listed lot numbers and expiration dates. Those taking this medication for cholesterol management are most at risk.
Check for the 30-count or 90-count bottles labeled with the product name Simvastatin USP 40mg, Rx only. Look for the specific lot numbers and expiration dates listed in the recall notice.
Reach out to PD-Rx Pharmaceuticals for specific instructions on how to handle the recalled product.
The recall states there were CGMP deviations, but does not specify if the product is unsafe. Consumers should contact PD-Rx for details.
Simvastatin 40mg tablets (Rx only) in 30-count or 90-count bottles with specific lot numbers and expiration dates listed in the recall notice.
Check the bottle for the lot numbers and expiration dates listed in the recall notice, which include specific production dates and quantities.
We’ve drafted a message you can send PD-Rx Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0561-2023 — PD-Rx Pharmaceuticals PD-Rx Pharmaceuticals Hello, I own a PD-Rx Pharmaceuticals that is covered by recall D-0561-2023 from PD-Rx Pharmaceuticals. 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.
