Preferred Pharmaceuticals recalls 40mg Simvastatin tablets (NDCs 68788-9868-9, 68788-9868-6, 68788-9868-3) due to cGMP deviations found during manufacturing inspections. Rx only products with specific lot numbers and expiration dates are affected.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 40mg Simvastatin tablets that were manufactured by Accord Healthcare. The recall is due to cGMP deviations found during manufacturing inspections, which could affect product safety.
The recall is due to cGMP deviations found during manufacturing inspections by Accord Healthcare. These deviations could potentially affect the quality and safety of the medication, though the exact risk is not specified in the recall notice.
People who have the recalled Simvastatin tablets (NDCs 68788-9868-9, 68788-9868-6, or 68788-9868-3) with specific lot numbers and expiration dates are affected. Patients on cholesterol-lowering medication are most at risk.
Check the product label for the NDC codes: 68788-9868-9, 68788-9868-6, or 68788-9868-3. The tablets are prescription-only and have specific lot numbers and expiration dates listed in the recall notice.
Look for the NDC codes 68788-9868-9, 68788-9868-6, or 68788-9868-3 on the bottle.
The recall is due to cGMP deviations found during manufacturing inspections by Accord Healthcare, which could affect product safety.
The recall notice does not specify a remedy or action for affected products.
Yes, the recall includes specific lot numbers and expiration dates listed in the product description.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0525-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0525-2023 from Preferred 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.
