Lupin Pharmaceuticals recalls 20mg Quinapril tablets due to N-Nitroso impurity exceeding safety limits. Affected lots may pose health risks. Contact for return instructions.
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Lupin Pharmaceuticals is recalling 20mg Quinapril tablets (90-pack) because they contain an impurity that could exceed safe levels. This recall affects prescription-only medication that was manufactured in specific lots and may pose health risks if taken.
The tablets contain N-Nitroso-quinapril impurities above the acceptable daily intake limit. This impurity could potentially cause health issues if taken in amounts exceeding safe levels, though the exact risk level isn't specified in the recall.
Prescription patients using Lupin's Quinapril 20mg tablets in the specific lot numbers mentioned. Those with high blood pressure who take this medication are most at risk.
Check for the product name 'Quinapril Tablets USP 20mg (90 pack)', prescription-only status, and lot number G102929 (expiring April 2023). The NDC code 68180-558-09 is also a key identifier.
Verify the product name, lot number, and expiration date to confirm if your tablets are affected.
The recall states there is a detection of N-Nitroso-quinapril impurity above acceptable limits, but the exact health risk isn't specified in the official notice.
Check for the lot number G102929 (expiring April 2023) and NDC code 68180-558-09 on your packaging.
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for further instructions.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0089-2023 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0089-2023 from Lupin. 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.
