Lidocaine recalls
Lidocaine products have been recalled 8 times, most recently on 29 Jul 2026. The recalling company is usually Novocol Pharmaceutical of Canada. The most common reason is packaging defects.
Total recalls8since 2013
Last 12 months2reported
Class I00% of total
Ongoing3latest 29 Jul 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 6 75%Class III 2 25%
Why lidocaine is recalled
Companies
Product types
By year
Ongoing lidocaine recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lidocaine HCl Injection, USP, 2%, 100 mg recalled by Fresenius Kabi USALidocaine | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Lidocaine HCI 2% and Epinephrine 1:100 recalledLidocaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS III | Lidocaine Patch 5%, 1 patch (63629-8755-20) recalledLidocaine | Bryant Ranch Prepack | Packaging Defects | Nationwide |
All lidocaine recalls, newest first
8 totalAbout 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.