Recall Ledger

Lidolog Kit recall (Asclemed USA Inc.)

DrugClass IIIOngoing

Summary: Asclemed USA Inc. is recalling 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.. Reason: Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan.

What is being 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.

Why

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

How serious is it

Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.

Where it was sold

Within U.S. - Tennessee (states named: Tennessee)

How to tell if yours is affected

Lot: 070126X1, Exp. 12/31/2027.

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0713-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass III
StatusOngoing
Recall startedJuly 15, 2026
ReportedJuly 29, 2026
CompanyAsclemed USA Inc.
Company locationTorrance, CA, United States
Initiated byVoluntary: Firm initiated
Quantity18 kits

More recalls from Asclemed USA Inc. · all drug recalls · recalls from July 2026

Official FDA record