PD-Rx Pharmaceuticals recalls 10mg Simvastatin tablets due to manufacturing quality issues. Affected lots expire by October 2023. Consumers should contact the company for details.
CGMP deviations.
PD-Rx Pharmaceuticals is recalling 10mg Simvastatin tablets that were manufactured with CGMP deviations. This means the product may not meet safety standards, so affected users should stop using it and contact the company.
CGMP deviations refer to manufacturing quality issues that could affect the product's safety and effectiveness. These deviations may mean the medication does not meet the required standards for quality control.
People who have the 10mg Simvastatin tablets with specific lot numbers and expiration dates listed in the recall notice. Those taking this medication for cholesterol management are most at risk.
Check the product label for the lot number and expiration date. The affected products include 30-count and 90-count bottles with specific lot numbers and expiration dates listed in the recall notice.
Look for the lot number and expiration date on the bottle to confirm if it's affected.
Reach out to PD-Rx Pharmaceuticals for further instructions on what to do with the product.
The recall is due to CGMP deviations, which are manufacturing quality issues that may affect the product's safety and effectiveness.
Affected lots include K22E32 (expiring 10/31/23), H22C33 (expiring 09/30/23), H22C81, J22C83, and K22E36 (expiring 10/31/23).
Check the product label for the lot number and expiration date. The affected products are 30-count and 90-count bottles with specific lot numbers listed in the recall notice.
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-0558-2023 — PD-Rx Pharmaceuticals PD-Rx Pharmaceuticals Hello, I own a PD-Rx Pharmaceuticals that is covered by recall D-0558-2023 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.
