Lorazepam recalls
Lorazepam products have been recalled 7 times, most recently on 6 Aug 2025. The recalling company is usually Hikma Pharmaceuticals USA. The most common reason is potency & assay.
Total recalls7since 2017
Last 12 months0reported
Class I114% of total
Ongoing1latest 6 Aug 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 14%Class II 6 86%Class III 0 0%
Why lorazepam is recalled
Companies
Product types
By year
Ongoing lorazepam recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lorazepam Injection, USP, 2 mg/mL, 25 x vials/carton recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
All lorazepam recalls, newest first
7 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lorazepam Injection, USP, 2 mg/mL, 25 x vials/carton recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lorazepam Injection, USP, 2mg/mL vial recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lorazepam Injection, USP, 2mg/mL vial, 25 vials recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lorazepam Injection, USP, 4mg/mL vial, 25 vial recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lorazepam Injection, USP, 2mg/mL vial, 25 vial recalledLorazepam | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS I | Lorazepam Oral Concentrate, USP, 2 mg/mL recalledLorazepam | Amneal Pharmaceuticals of New York | Other | Nationwide |
| Drug | CLASS II | Lorazepam Tablets, USP CIV, 5 mg recalled by Leading PharmaLorazepam | Leading Pharma | Other | 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.