RecallRadar

FDA Drug recall D-0713-2026

Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmac…

On 2026-07-29 the FDA classified a Class III recall of Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmac… by Asclemed Usa, citing labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0713-2026
ClassificationClass III
Statusongoing
Initiated2026-07-15
Published2026-07-29
Last updated2026-09-13 11:52 UTC
CompanyAsclemed Usa
DistributionTN

Product

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

Identifiers

ndc76420-760-01
ndc55150-164-02
ndc70121-1049-5
ndc67777-419-02
code_infoLot: 070126X1, Exp. 12/31/2027.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0713-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.