Harvard Drug Group recalls 30mg Nifedipine extended-release tablets (NDC 0904-7080-61 and 0904-7080-06) due to failed dissolution testing. These prescription-only medications may not release properly in the body.
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
The Harvard Drug Group is recalling prescription 30mg Nifedipine extended-release tablets that failed dissolution testing. This means the medication might not work as intended when taken, potentially causing ineffective blood pressure control.
The tablets failed dissolution testing, meaning they may not release the medication properly in the body. This could lead to inconsistent blood pressure control. However, the recall does not indicate immediate harm to users.
Prescription holders who have the specific 30mg Nifedipine extended-release tablets with NDC numbers 0904-7080-61 or 0904-7080-06. Patients taking blood pressure medication are most at risk of ineffective treatment.
Check for 30mg Nifedipine extended-release tablets in unit dose cartons with NDC 0904-7080-61 (100-count) or NDC 0904-7080-06 (50-count). These were distributed by Harvard Drug Group with specific expiration dates.
Identify your specific NDC numbers to confirm if your tablets are recalled.
The recall indicates the tablets may not release properly, but the official notice does not state they cause immediate harm. They are prescription-only and should be used as directed.
Look for NDC numbers 0904-7080-61 (100-count carton) or 0904-7080-06 (50-count carton) on the packaging.
The recall does not specify a stop-use instruction, so you can continue using them if you have a prescription. However, contact your doctor for advice.
We’ve drafted a message you can send The Harvard Drug Group to request your refund or repair — edit it as you like.
Subject: Recall D-0652-2021 — The Harvard Drug Group The Harvard Drug Group Hello, I own a The Harvard Drug Group that is covered by recall D-0652-2021 from The Harvard Drug Group. 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.
