Argatroban recalls
Argatroban products have been recalled 2 times, most recently on 28 Oct 2026. The recalling company is usually Par Health USA. The most common reason is particulate matter.
Total recalls2since 2026
Last 12 months2reported
Class I2100% of total
Ongoing2latest 28 Oct 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 100%Class II 0 0%Class III 0 0%
Why argatroban is recalled
Companies
Product types
By year
Ongoing argatroban recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | Nationwide |
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | Nationwide |
All argatroban recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | Nationwide |
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | 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.