Preferred Pharmaceuticals recalls Losartan Potassium & HCTZ 50mg/12.5mg tablets with AZIDO impurities above safe levels. Consumers should check lot numbers and contact the company for details.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Preferred Pharmaceuticals is recalling Losartan Potassium & HCTZ tablets due to unsafe levels of an impurity called AZIDO. This could pose a health risk if taken as directed.
The tablets contain AZIDO impurities at levels above what's safe. This impurity could cause health issues if the medication is taken as intended.
People who have the specific lot numbers listed (K1721D or K1021E) for the 90-tablet package. Those taking blood pressure medication may be at risk.
Check the lot number on the packaging: K1721D (expires 4/30/2023) or K1021E (expires 7/31/2023). The product is a 90-tablet package with NDC 68788-7758-09.
Look for lot numbers K1721D or K1021E on the packaging.
The recall mentions AZIDO impurities at levels above acceptable limits, but does not specify the exact amount or health effects.
Check the lot number on the packaging: K1721D (expires 4/30/2023) or K1021E (expires 7/31/2023).
The recall does not specify a remedy, so contact Preferred Pharmaceuticals directly for guidance.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0891-2022 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0891-2022 from Preferred 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.
