Preferred Pharmaceuticals recalls 80mg Simvastatin tablets (NDC 68788-9429-9) manufactured by Accord Healthcare due to cGMP deviations. No specific remedy is stated in the recall notice.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 80mg Simvastatin tablets that were manufactured by Accord Healthcare. The recall is due to manufacturing deviations found during quality control inspections. This affects prescription-only medication that was sold between specific dates and lots.
The recall is based on cGMP (Current Good Manufacturing Practice) deviations found during quality inspections at Accord Healthcare's facility. These deviations indicate potential issues with the manufacturing process that could affect the safety and quality of the medication.
Prescription holders of the 80mg Simvastatin tablets with NDC 68788-9429-9 and specific lots (B0222S, F1121B, G2721L) are affected. Patients taking this medication for cholesterol management are most at risk.
Check for the product name 'Simvastatin Tablets, USP, 80 mg, 90-count bottle' with NDC 68788-9429-9. Look for specific lot numbers: B0222S (expires 2/29/2024) or F1121B, G2721L (expires 11/30/2023).
Identify the NDC number 68788-9429-9 and lot numbers B0222S, F1121B, or G2721L on the packaging.
The recall is due to cGMP deviations found during quality inspections at Accord Healthcare's manufacturing facility.
The recall notice does not specify a remedy, so no action is required beyond checking if your product matches the described details.
The recall is based on manufacturing deviations, but no specific safety risks are described in the notice.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0523-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0523-2023 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.
