Accord Healthcare recalls 8 mg Doxazosin tablets due to FDA inspection finding CGMP deviations. Affected products include 100-tablet and 1,000-tablet packs with specific NDC and UPC numbers. No remedy provided in recall notice.
CGMP Deviations: recalling drug products following an FDA inspection.
Accord Healthcare is recalling 8 mg Doxazosin tablets that were manufactured following an FDA inspection finding quality control issues. This recall affects specific packaging sizes and batch numbers, but no action is required by consumers as the recall notice does not specify a remedy.
The recall is triggered by FDA inspections identifying deviations in current Good Manufacturing Practices (CGMP) for the drug. This means the tablets may not meet quality standards, but the specific risk to consumers is not detailed in the recall notice.
Prescription drug users who have the recalled Doxazosin tablets with specific NDC and UPC numbers. Patients taking this medication should check their packaging for the affected batch numbers.
Check your Doxazosin tablets for the NDC 16729-415-01 (100 tablets) or NDC 16729-415-17 (1,000 tablets) with the listed UPC codes. The affected batches include R2200672, R2200673, R2201097 for the 100-tablet packs and R2200678 for the 1,000-tablet packs.
Look for the NDC 16729-415-01 or 16729-415-17 on the packaging to identify affected tablets.
The recall notice does not specify a remedy, so no action is required by consumers.
Affected batches include R2200672, R2200673, R2201097 for 100-tablet packs and R2200678 for 1,000-tablet packs.
Check the NDC and UPC numbers on your packaging; affected products have specific NDC codes and batch numbers listed in the recall notice.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0389-2023 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0389-2023 from Accord Healthcare. 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.
