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Health & beauty United States Recall (ongoing)

Asclemed USA Inc. recalls Lidolog Kit

Lidolog Kit (contains Lidocaine HCl Injection, USP, 2% 2 mL vial; NDC 76420-760-01; Lot 070126X1, exp. 12/31/2027) distributed by Enovachem Pharmaceuticals and recalled by Asclemed USA Inc. was sold in Tennessee (18 kits). The kit is recalled because the label wrap covers the barcode, making it hard to scan.

What's being 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.

Recalling firm: Asclemed USA Inc., Torrance, CA, United States.

How to identify it

Lot: 070126X1, Exp. 12/31/2027.

The hazard

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

What to do

Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.

The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.

Where it was sold

Within U.S. - Tennessee

The official notice

This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.

Read the official notice (opens in a new tab)

A little guidance

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