Class III · Lower riskActive recall
Lidolog Kit
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byAsclemed USA, Inc.
| Brand name | LIDOLOG KIT |
| Generic name | LIDOCAINE, KENALOG, POVIDONE IODINE |
| Distributed by / for | Eugia US LLC |
| NDC | 55150-164-02 |
Show the full FDA record
| Full product label | 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 |
| Recalling firm | Eugia US LLC |
| Distribution | US Nationwide. |
| Quantity | 168,300 vials |
| Recall initiated | 2026-05-18 |
| Report date | 2026-06-10 |
| Recall completed | — |
| Recall number | D-0552-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | East Windsor NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.