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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: 070126X1, Exp. 12/31/2027.
Where it was soldWithin U.S. - Tennessee
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

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byAsclemed USA, Inc.
Brand nameLIDOLOG KIT
Generic nameLIDOCAINE, KENALOG, POVIDONE IODINE
Distributed by / forEnovachem Pharmaceuticals, Torrance, CA 90501
NDC76420-760-01
Show the full FDA record
Full product labelLidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-760-01.
Recalling firmAsclemed USA Inc.
DistributionWithin U.S. - Tennessee
Quantity18 kits
Recall initiated2026-07-15
Report date2026-07-29
Recall completed—
Recall numberD-0713-2026
ClassificationClass III
FDA statusOngoing
Origin on fileTorrance CA United States

Related

Recent drug recallsCheck another medication

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.