Preferred Pharmaceuticals is recalling 10mg Atorvastatin Calcium Tablets (NDC 68788-7630-9) manufactured by Accord Healthcare due to quality control deviations. This recall affects specific batches with lot numbers A0523D, F14220, and J0622Q.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 10mg Atorvastatin Calcium Tablets that were manufactured by Accord Healthcare. The recall is due to quality control issues identified during manufacturing inspections. This affects prescription-only medication bottles with specific lot numbers and expiration dates.
The recall is based on manufacturing quality control deviations found during inspections by Accord Healthcare. These deviations indicate potential issues with the production process that could affect the medication's safety and effectiveness. However, the specific risk to patients is not clearly described in the recall notice.
Prescription holders of the 10mg Atorvastatin Calcium Tablets with lot numbers A0523D, F14220, or J0622Q are affected. Patients taking this medication should check their specific batch details.
Check the product label for the lot number: A0523D, F14220, or J0622Q. The medication is a prescription-only 10mg Atorvastatin Calcium Tablets bottle with NDC 68788-7630-9.
Look for the lot number on the bottle: A0523D, F14220, or J0622Q.
The recall is due to quality control deviations found during manufacturing inspections by Accord Healthcare.
Check the lot number on the bottle. If it matches A0523D, F14220, or J0622Q, contact Preferred Pharmaceuticals for instructions.
The recall notice does not specify a risk of serious injury or harm to patients.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0511-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0511-2023 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.
