Esperion recalls
Esperion has 2 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 24 Apr 2024. The most frequent reason is potency & assay.
Total recalls2since 2023
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Apr 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 2 100%
Why esperion is recalled
Product types
By year
All esperion recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Nexlizet (bempedoic acid and ezetimibe) tablets, 180 mg/10 mg recalledNexlizet | Esperion | Potency & Assay | Nationwide |
| Drug | CLASS III | Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg recalled by EsperionNexlizet | Esperion | Potency & Assay | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.