Numbing recalls
The FDA has published 1 recall involving Numbing since 2026. The latest was reported on 18 Feb 2026. 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 2026
Last 12 months1reported
Class I00% of total
Ongoing1latest 18 Feb 2026
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 numbing is recalled
Companies
By year
Ongoing numbing recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | For Sensitive Skin, 4% Lidocaine, [ or] recalledPro Numb Sensitive Skin | Pro Numb Tattoo Numbing Spray | Manufacturing (CGMP) Deviations | Nationwide |
All numbing recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | For Sensitive Skin, 4% Lidocaine, [ or] recalledPro Numb Sensitive Skin | Pro Numb Tattoo Numbing Spray | Manufacturing (CGMP) Deviations | Nationwide |
Should you stop taking Numbing?
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.