Epinephrine-lidocaine recalls
The FDA has published 5 recalls involving Epinephrine-lidocaine since 2023. The latest was reported on 30 Jul 2025. Most were for potency & assay. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls5since 2023
Last 12 months0reported
Class I00% of total
Ongoing3latest 30 Jul 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 60%Class III 2 40%
Why epinephrine-lidocaine is recalled
Companies
By year
Ongoing epinephrine-lidocaine recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Sterility | Nationwide |
| Drug | CLASS II | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Sterility | Nationwide |
| Drug | CLASS III | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | Nationwide |
All epinephrine-lidocaine recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, mL Vials recalled | Imprimis Njof | Potency & Assay | Nationwide |
| Drug | CLASS II | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Sterility | Nationwide |
| Drug | CLASS II | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Sterility | Nationwide |
| Drug | CLASS III | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | Nationwide |
| Drug | CLASS III | Epinephrine-Lidocaine HCl (0.25mg/mL recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | Nationwide |
Should you stop taking Epinephrine-lidocaine?
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.