US Drug Recall Register
Class III · Low risk Ongoing Initiated Jul 15, 2026 (2 months ago)

Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

What was recalled

Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-760-01.

Recalling firm
Asclemed USA Inc.
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0713-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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