Lidolog Kit
Lidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
Contact your healthcare provider or pharmacy if you have concerns about the product's labeling or scanning, and do not rely on the barcode for identification if it is obscured.
Why it was recalled
The Lidolog Kit is being recalled because the label wrap covers the barcode, which prevents it from being scanned properly. This issue affects kits containing 2mL vials of 2% Lidocaine HCl injection.
Is mine affected?
Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.
Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only
- NDC / UPC
- NDC 76420-760-01
Official source
Other recent recalls from Asclemed USA Inc.
Editorial summary by Recall Canary · last updated 2026-07-22 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification