RemedyRepack Inc. recalls Doxazosin 2mg tablets (NDC 70518-1560-00/01) due to cGMP deviations. Affected lots expire by 12/31/2023 or 05/31/2024. Consumers should check their bottle labels for specific lot numbers.
cGMP Deviations
RemedyRepack Inc. is recalling Doxazosin 2 mg tablets in 30-count and 90-count bottles due to manufacturing quality control issues. This recall affects patients who have these specific lot numbers and may pose a risk of incorrect dosing or ineffective medication.
The recall is due to cGMP (current Good Manufacturing Practice) deviations, which means the tablets were produced without following proper quality control standards. This could lead to incorrect dosing or ineffective medication, but it does not indicate immediate safety risks like injury or death.
Patients prescribed Doxazosin 2 mg tablets by a healthcare provider who have the recalled 30-count or 90-count bottles with specific lot numbers. Those most at risk are individuals taking the medication for blood pressure or prostate issues.
Check your Doxazosin 2 mg tablets for the following: 30-count bottles (NDC 70518-1560-00) or 90-count bottles (NDC 70518-1560-01) with lot numbers listed in the recall notice. The expiration dates for these lots range from 08/31/2023 to 05/31/2024.
Look for the product name, dosage, and lot number on the bottle label to confirm if it matches the recalled items.
If you have the recalled lot numbers, inform your doctor or pharmacist about the recall to discuss alternative medications.
RemedyRepack Inc. is recalling Doxazosin 2 mg tablets in 30-count and 90-count bottles due to cGMP deviations in manufacturing.
Check the lot number on your bottle label. The recalled lots have specific expiration dates: 08/31/2023 to 05/31/2024 for the 30-count and 90-count bottles.
No, the recall does not require immediate discontinuation. However, if you have the affected lot numbers, contact your healthcare provider for alternative options.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0492-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0492-2023 from RemedyRepack. 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.
