Lupin Pharmaceuticals recalls 2.5mg/10mg capsules with wrong expiry date (Feb 2027 instead of Jan 2027). Discard or contact for replacement.
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
Lupin Pharmaceuticals is recalling amlodipine and benazepril capsules due to incorrect expiry dates. This could lead to medication safety issues if the capsules are used after the wrong expiration date.
The capsules were labeled with an incorrect expiration date (Feb 2027 instead of Jan 2027). Using expired medication could lead to ineffective treatment or safety risks.
People who have the 100-capsule bottle with lot number GB01616, manufactured for Lupin Pharmaceuticals. Those taking blood pressure medication are most at risk.
Check for the lot number GB01616 on the bottle. The product is a 2.5 mg/10 mg amlodipine and benazepril capsule bottle sold by prescription.
Verify the expiration date on the bottle label. If it shows February 2027 instead of January 2027, it is recalled.
The capsules were labeled with an incorrect expiration date (February 2027 instead of January 2027).
Look for the lot number GB01616 on the bottle. The product is a 2.5 mg/10 mg amlodipine and benazepril capsule bottle sold by prescription.
The recall record does not specify a remedy, so contact Lupin Pharmaceuticals for guidance.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0542-2025 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0542-2025 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.
