RecallRadar

FDA Drug recall D-0552-2026

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ…

On 2026-06-10 the FDA classified a Class III recall of Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ… by Eugia Us, 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-0552-2026
ClassificationClass III
Statusongoing
Initiated2026-05-18
Published2026-06-10
Last updated2026-09-13 11:52 UTC
CompanyEugia Us
DistributionUS

Product

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02

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, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029

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-0552-2026%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.