Levocarnitine recalls
Levocarnitine products have been recalled 1 time, most recently on 6 May 2026. The recalling company is usually American Regent. The most common reason is labeling errors.
Total recalls1since 2026
Last 12 months1reported
Class I00% of total
Ongoing1latest 6 May 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 1 100%
Why levocarnitine is recalled
Companies
Product types
By year
Ongoing levocarnitine recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Levocarnitine Injection, USP (200 mg/mL) Single-Dose Vial recalledLevocarnitine | American Regent | Labeling Errors | Nationwide |
All levocarnitine recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Levocarnitine Injection, USP (200 mg/mL) Single-Dose Vial recalledLevocarnitine | American Regent | Labeling Errors | 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.