Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Losartan HCTZ 100/12.5 mg Recalled by RemedyRepack Inc. Due to CGMP Deviations- AZIDO Impurity levels observed to be...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact RemedyRepack Inc. directly.
Affected Products
Losartan HCTZ 100/12.5 mg, 90 count bottles NDC# 70518-2564-00 Repackaged NDC Original NDC # 68180-0216-09
Quantity: 30 bottles/90 count = 2,700 tablets
Why Was This Recalled?
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Where Was This Sold?
This product was distributed to 3 states: FL, SC, VA
About RemedyRepack Inc.
RemedyRepack Inc. has 60 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report