Losartan is an ARB blood pressure medication. We track every FDA enforcement recall involving Losartan (Cozaar) — 36 recalls in our database, including 4 active.
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MACLEODS PHARMA USA, INC — Presence of foreign substance: plastic-like substance.
Recall D-0498-2024
Strides Pharma Inc. — Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Recall D-0895-2023
Macleods Pharma Usa Inc — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-1164-2022
PD-Rx Pharmaceuticals, Inc. — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-1162-2022
PD-Rx Pharmaceuticals, Inc. — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-1163-2022
PD-Rx Pharmaceuticals, Inc. — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-1161-2022
Strides Pharma Inc. — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-0973-2022
Strides Pharma Inc. — CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall D-0974-2022
Showing 8 of 36. See all Losartan recalls.
This page is for information only and isn’t medical advice. Always follow your clinician’s guidance.
The FDA publishes recalls, but most never make the news. The reliable way is an automated alert: sign up free and we’ll email you when a Losartan recall is issued.
Most prescriptions filled in the US are generics, so most recalls involve generic products. A recall doesn’t mean the drug itself is unsafe — it usually affects specific lots or manufacturers.
Yes — weekly recall alert digests are free forever, with no credit card required. See pricing.