Taurine recalls
The FDA has published 10 recalls involving Taurine since 2012. 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 recalls10since 2012
Last 12 months0reported
Class I00% of total
Ongoing3latest 15 Oct 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 10 100%Class III 0 0%
Why taurine is recalled
Companies
By year
Ongoing taurine recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Taurine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Taurine 50 mg/mL. Compounded by Tri-Coast Pharmacy recalled | Tri-Coast Pharmacy | Sterility | Nationwide |
| Drug | CLASS II | Taurine 100 mg/ml Injection, compounded by Olympia Pharmacy recalled | Lowlite Investments | Sterility | Nationwide |
All taurine recalls, newest first
10 totalShould you stop taking Taurine?
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.