Preferred Pharmaceuticals recalls 5mg Rosuvastatin tablets (NDC 68788-7971-3) due to manufacturing quality deviations. Consumers should contact the company for details on affected lots and next steps.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 5mg Rosuvastatin tablets that were manufactured by Accord Healthcare. The recall is due to quality control issues found during manufacturing inspections. This affects people who have the specific lot numbers listed in the recall notice.
The recall is due to manufacturing quality deviations found at Accord Healthcare after their inspection. This means the tablets may not meet the required safety and quality standards, but the exact risk to consumers is not specified in the notice.
People who have the specific lot numbers of Rosuvastatin tablets (5mg, 30-count) from Preferred Pharmaceuticals. Those with the listed lot numbers are most at risk.
Check the product label for the lot numbers: A1723C (exp 8/31/2025), A1922B (exp 6/30/2024), D0622M, F2922I (exp 7/31/2024), G3021L (exp 1/31/2024), H2622P and J0722C (exp 10/31/2024).
Look for the lot numbers listed in the recall notice to determine if your tablets are affected.
The recall is due to manufacturing quality deviations found at Accord Healthcare after their inspection.
The official notice does not specify a remedy, so contact Preferred Pharmaceuticals for details on affected lots and next steps.
Yes, check for lot numbers: A1723C (exp 8/31/2025), A1922B (exp 6/30/2024), D0622M, F2922I (exp 7/31/2024), G3021L (exp 1/31/2024), H2622P and J0722C (exp 10/31/2024).
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0520-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0520-2023 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.
