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Lidocaine HCl Injection 2%
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DRUG RECALLLOW

Lidocaine HCl Injection 2%

Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.

What to do

Healthcare providers should inspect their inventory and contact the manufacturer or distributor for return instructions if the barcode is obscured.

Recalled
Listed
Updated
Recall No.
D-0552-2026
Agency
FDA
Firm
Eugia US LLC
Recall ID
99024
Status
ONGOING

Recall at a glance

Quantity recalled
168,300 vials

Why it was recalled

Eugia US LLC is recalling this injectable anesthetic because the label wrap covers the barcode, which prevents the product from being scanned correctly. This issue affects the 2 mL single-dose vials.

Is mine affected?

Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

Lidocaine HCl Injection, USP 2%

Lot code
3LC26029A, Feb-2029, 3LC26031A, Mar-2029
Strength
40 mg
NDC / UPC
NDC 55150-164-02

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification