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.
Recall at a glance
- Quantity recalled
- 18 kits
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 OnlyNDC / UPC: NDC 76420-760-01
| Lot code |
|---|
| – |
| 070126X1, 2027 |
Where it was sold
Distributed in Tennessee.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Labeling Error recalls
Other recent recalls from Asclemed USA Inc.
Editorial summary by Recall Canary · summary updated 2026-07-22 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification