Why it was recalled
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Product 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
Lot numbers, UPCs & expiration codes
Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
Where it was sold
US Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0552-2026
- Classification
- Class III
- Status
- Ongoing
- Recall initiated
- May 18, 2026
- FDA report date
- Jun 10, 2026
- Quantity
- 168,300 vials
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Eugia US LLC
Original FDA data
Every field from FDA enforcement report D-0552-2026, exactly as published.
Show all FDA fields
- City
- East Windsor
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 99024
- Address
- 279 Princeton Hightstown Rd
- Code information
- Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
- Postal code
- 08520-1401
- Report date
- Jun 10, 2026
- Product type
- Drugs
- Recall number
- D-0552-2026
- Classification
- Class III
- Recalling firm
- Eugia US LLC
- 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
- Product 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
- Distribution pattern
- US Nationwide.
- Recall initiation date
- May 18, 2026
- Initial firm notification
- Letter
- Center classification date
- May 29, 2026