Lidocaine Wound (benzalkonium Chloride recalls
The FDA has published 1 recall involving Lidocaine Wound (benzalkonium Chloride since 2026. The latest was reported on 6 May 2026. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2026
Last 12 months1reported
Class I00% of total
Ongoing1latest 6 May 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 1 100%
Why lidocaine wound (benzalkonium chloride is recalled
Companies
By year
Ongoing lidocaine wound (benzalkonium chloride recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Lidocaine Wound Gel (Benzalkonium Chloride recalled | Water-Jel Technologies | Other | Nationwide |
All lidocaine wound (benzalkonium chloride recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Lidocaine Wound Gel (Benzalkonium Chloride recalled | Water-Jel Technologies | Other | Nationwide |
Should you stop taking Lidocaine Wound (benzalkonium Chloride?
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.