Where's it on?
FDA · Drugs ·

Lidolog Kit recall

Asclemed USA Inc. recalled Lidolog Kit on July 29, 2026 because of labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan. It was sold in TN.

Why it was recalled

Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

What's recalled

Lidolog 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.

Quantity: 18 kits

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Asclemed USA Inc., Torrance, CA
Date
Severity
Class III
the product is unlikely to cause health problems but breaks a rule.
Where sold
TN
Within U.S. - Tennessee
Status
Ongoing
Recall number
D-0713-2026
Source
U.S. Food and Drug Administration

More drugs recalls

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops
· Sterling Pharmaceutical Services LLCAvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops
· Sterling Pharmaceutical Services LLCClear Eyes Redness Relief
· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare companyAvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops
· Sterling Pharmaceutical Services LLCLubricant Eye Drops-Cameron Pharmaceuticals
· Sterling Pharmaceutical Services LLCReliable -1 Laboratories
· Sterling Pharmaceutical Services LLC