Macleods Pharma USA recalls 10mg/20mg blood pressure tablets (NDC 33342-192-07) manufactured in India with cGMP deviations. Consumers should check lot numbers and contact the company for details.
cGMP deviations
Macleods Pharma recalls certain blood pressure tablets due to manufacturing quality issues. This recall affects people who have the specific 10mg/20mg tablets with the listed lot number and expiration date. The issue means the tablets may not be safe to use as intended.
The tablets were made with cGMP (current Good Manufacturing Practice) deviations, which means the production process didn't meet safety and quality standards. This could lead to the tablets not working properly or being unsafe for use.
People who have the 10mg/20mg blood pressure tablets with lot number BAD62101A and expiration date 02/2024 are affected. Those taking these medications for high blood pressure are most at risk.
Check for the product name 'Amlodipine and Olmesartan Medoxomil Tablets', 10mg/20mg, 30-count bottles, Rx only. Look for the lot number BAD62101A and expiration date 02/2024 on the packaging.
Look for the lot number BAD62101A and expiration date 02/2024 on the packaging.
The recall states there were cGMP deviations, which means the tablets may not be safe to use as intended. The manufacturer recommends checking if you have the affected lot number.
Check for the product name 'Amlodipine and Olmesartan Medoxomil Tablets', 10mg/20mg, 30-count bottles, Rx only with lot number BAD62101A and expiration date 02/2024.
The recall does not specify a remedy, so contact Macleods Pharma USA for further instructions.
We’ve drafted a message you can send Macleods to request your refund or repair — edit it as you like.
Subject: Recall D-0632-2022 — Macleods Macleods Hello, I own a Macleods that is covered by recall D-0632-2022 from Macleods. 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.
