L-carnitine recalls
The FDA has published 11 recalls involving L-carnitine since 2013. The latest was reported on 15 Oct 2025. Most were for sterility. Medaus has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls11since 2013
Last 12 months1reported
Class I00% of total
Ongoing2latest 15 Oct 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 11 100%Class III 0 0%
Why l-carnitine is recalled
Companies
By year
Ongoing l-carnitine recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | L-Carnitine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | L-Carnitine 250 mg/mL. Compounded by Tri-Coast Pharmacy recalled | Tri-Coast Pharmacy | Sterility | Nationwide |
All l-carnitine recalls, newest first
11 totalShould you stop taking L-carnitine?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.