Northwind Pharmaceuticals recalls 7.5mg BusPIRone Hydrochloride tablets due to CGMP deviations. Affected lots: NDC 51655-511-52, Lot F117312201, expiring June 30, 2024.
CGMP Deviations
Northwind Pharmaceuticals is recalling 7.5mg BusPIRone Hydrochloride tablets that were repackaged by their company. The recall is due to CGMP deviations, which means the product may not meet quality standards.
CGMP deviations refer to failures in the manufacturing quality control processes. This could mean the tablets may not meet the required safety and quality standards for prescription drugs.
Prescription holders of the 7.5mg BusPIRone Hydrochloride tablets with NDC 51655-511-52 and Lot F117312201 are affected. Patients using these specific tablets are most at risk.
Check for the NDC code 51655-511-52 and Lot number F117312201 on the bottle. The tablets are prescription-only and expire June 30, 2024.
Look for NDC 51655-511-52 and Lot F117312201 on the bottle label.
Northwind Pharmaceuticals is recalling 7.5mg BusPIRone Hydrochloride tablets due to CGMP deviations.
Check for NDC 51655-511-52 and Lot F117312201 on the bottle label.
The recall record does not specify a remedy, so contact Northwind Pharmaceuticals for guidance.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0549-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0549-2023 from Northwind 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.
