Preferred Pharmaceuticals is recalling 4 mg Glimepiride Tablets (90-count) manufactured by Accord Healthcare due to quality control deviations found during inspections. This is a prescription-only medication.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 4 mg Glimepiride Tablets (90-count bottles) because manufacturing quality issues were found at the production facility. This recall affects prescription-only diabetes medication that may not be safe for patients.
The recall is due to quality control deviations found during manufacturing inspections at Accord Healthcare. These deviations could potentially affect the safety and effectiveness of the medication, though the specific risk is not detailed in the recall notice.
Prescription holders of Glimepiride Tablets (4 mg, 90-count) manufactured by Accord Healthcare in Durham, NC. Patients with diabetes who require this medication are most at risk.
Check for the product name 'Glimepiride Tablets USP, 4 mg, 90-count bottle', prescription-only status, and the lot numbers H1221Z, I0121J, or J0622X with expiration date 10/31/2023.
Verify the product name, lot numbers, and expiration date to confirm if your medication is recalled.
The recall states there were manufacturing quality deviations, but does not specify if the medication is unsafe. Patients should check the recall details to confirm.
Check for the product name 'Glimepiride Tablets USP, 4 mg, 90-count bottle', prescription-only status, and lot numbers H1221Z, I0121J, or J0622X with expiration date 10/31/2023.
The recall does not specify a remedy, so you should check with your healthcare provider or the manufacturer for guidance.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0527-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0527-2023 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.
