Lupin Pharmaceuticals recalls 10 mg Lisinopril tablets with a metal piece embedded in one tablet. This could cause injury if swallowed. Consumers should contact the company for details.
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Lupin Pharmaceuticals is recalling 10 mg Lisinopril tablets that may contain a metal piece. This foreign material could cause injury if swallowed, so affected consumers should stop using the tablets and contact the company.
A small metal piece is embedded in one tablet. If swallowed, it could cause injury or internal damage. This is a foreign object hazard.
People who have the 1000-count bottles of Lisinopril 10 mg tablets, Rx Only, manufactured by Lupin Pharmaceuticals Inc. in Baltimore, Maryland. Those taking blood pressure medication are most at risk.
Check for the product name 'Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only'. The lot number is Q201182 with an expiration date of March 2024.
If you have the recalled 1000-count bottles of Lisinopril 10 mg tablets, stop using them immediately.
Contact Lupin Pharmaceuticals for instructions on how to return the tablets or get a replacement.
The recall is for tablets that may contain a metal piece. Swallowing this could cause injury, but the risk is low as only one tablet is affected.
Check for the product name 'Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only' with lot number Q201182 and expiration date March 2024.
Stop using the tablets and contact Lupin Pharmaceuticals for instructions on returning them or getting a replacement.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1536-2022 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1536-2022 from Lupin 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.
