Let (lidocaine recalls
The FDA has published 1 recall involving Let (lidocaine since 2023. The latest was reported on 13 Dec 2023. Most were for packaging defects. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2023
Last 12 months0reported
Class I00% of total
Ongoing0latest 13 Dec 2023
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 let (lidocaine is recalled
Companies
By year
All let (lidocaine recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine recalled | Right Value Drug Stores | Packaging Defects | Nationwide |
Should you stop taking Let (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.