HIGHFDA DRUG

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

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

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
May 18, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 18, 2026
Hazard Level
HIGH
Brands
LIDOLOG KIT, Asclemed USA, Inc.
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
LIDOLOG KIT, Asclemed USA, Inc.
Model numbers
Lot, expiry: Lot 3LC26029A, exp Feb-2029, Lot 3LC26031A, exp Mar-2029
UPC codes
76420-760, 76420-760-01, 55150-164-02, 70121-1049-5, 67777-419-02
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 18, 2026

  2. Reported by FDA DRUG

    June 10, 2026

  3. RecallRadar source check

    June 16, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Eugia US LLC or your healthcare provider for guidance. Notification method: Letter

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Full Description

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. Generic: LIDOCAINE, KENALOG, POVIDONE IODINE; Brand: LIDOLOG KIT. Reason: Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan. Classification: Class III. Quantity: 168,300 vials. Distribution: US Nationwide.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot
expiry: Lot 3LC26029A
exp Feb-2029
Lot 3LC26031A
exp Mar-2029
UPC Codes
76420-760
76420-760-01
55150-164-02
+2 more
Affected States
ALL
Report Date
June 10, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE