Direct Rx recalls Losartan Pot/HCTZ 50/12.5 mg tablets (NDC 72189-297-90) due to AZIDO impurities exceeding safety limits. Affected lots expire 1/31/25.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .
Direct Rx is recalling Losartan Pot/HCTZ 50/12.5 mg tablets (NDC 72189-297-90) because they contain AZIDO impurities above acceptable levels. This could pose a health risk if taken as directed.
The recall is for AZIDO impurities found in the medication that exceed safe levels. While the exact health risk isn't specified, impurities like this can cause health issues when taken as directed.
People who purchased these specific lots of Losartan Pot/HCTZ tablets from Direct Rx in the U.S. are affected. Those with hypertension or heart conditions requiring this medication are most at risk.
Check for the NDC code 72189-297-90 on the packaging. The affected lots include numbers 19NO2108, 19NO2114, and 22NO2126, expiring January 31, 2025.
Look for the NDC code 72189-297-90 and lot numbers 19NO2108, 19NO2114, or 22NO2126 on the packaging.
The recall states AZIDO impurities exceed safe levels, but the official notice doesn't specify if it's safe to take.
Check for NDC 72189-297-90 and lot numbers 19NO2108, 19NO2114, or 22NO2126 on the packaging.
The recall doesn't specify a remedy, so contact Direct Rx for guidance.
We’ve drafted a message you can send Direct Rx to request your refund or repair — edit it as you like.
Subject: Recall D-0894-2022 — Direct Rx Direct Rx Hello, I own a Direct Rx that is covered by recall D-0894-2022 from Direct Rx. 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.
