Lidopatch (lidocaine recalls
The FDA has published 1 recall involving Lidopatch (lidocaine since 2020. The latest was reported on 3 Jun 2020. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2020
Last 12 months0reported
Class I00% of total
Ongoing1latest 3 Jun 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why lidopatch (lidocaine is recalled
Companies
By year
Ongoing lidopatch (lidocaine recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch recalled | Wuhan Bingbing Pharmaceutical | Manufacturing (CGMP) Deviations | Nationwide |
All lidopatch (lidocaine recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch recalled | Wuhan Bingbing Pharmaceutical | Manufacturing (CGMP) Deviations | Nationwide |
Should you stop taking Lidopatch (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.