FDA DrugsClass III
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Via...
Published: June 10, 2026Recall ID: D-0552-2026Category: drugsCountry: US
Reason for Recall / Hazard
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Product Description & Identification
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
Affected Products
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
Additional Source Details
| Field | Value |
|---|---|
| City | East Windsor |
| State | NJ |
| Openfda › Route › 1 | EPIDURAL |
| Openfda › Route › 2 | INFILTRATION |
| Openfda › Route › 3 | INTRA-ARTICULAR |
| Openfda › Route › 4 | INTRAMUSCULAR |
| Openfda › Route › 5 | TOPICAL |
| Openfda › Rxcui › 1 | 797730 |
| Openfda › Rxcui › 2 | 1737757 |
| Openfda › Rxcui › 3 | 1792144 |
| Openfda › Spl id | 47db1f9e-f201-2918-e063-6394a90a82e9 |
| Openfda › Brand name | LIDOLOG KIT |
| Openfda › Spl set id | 069e145d-7992-4f56-9fcb-20782ecc2d53 |
| Openfda › Package ndc › 1 | 76420-760-01 |
| Openfda › Package ndc › 2 | 55150-164-02 |
| Openfda › Package ndc › 3 | 70121-1049-5 |
| Openfda › Package ndc › 4 | 67777-419-02 |
| Openfda › Product ndc | 76420-760 |
| Openfda › Generic name | LIDOCAINE, KENALOG, POVIDONE IODINE |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Manufacturer name | Asclemed USA, Inc. |
| Openfda › Is original packager | true |
| Event id | 99024 |
| Address 1 | 279 Princeton Hightstown Rd |
| Code info | Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029 |
| Postal code | 08520-1401 |
| Report date | 20260610 |
| Product type | Drugs |
| Product quantity | 168,300 vials |
| Reason for recall | Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260518 |
| Initial firm notification | Letter |
| Center classification date | 20260529 |
Overview
- Recalling FirmEugia US LLC
- StatusOngoing
- Risk LevelClass III
- DistributionUS Nationwide.