Asclemed USA Inc.: Lidolog Kit, Kit
Recall Summary Asclemed USA Inc. is recalling Lidolog Kits containing lidocaine injection distributed in Tennessee because the product label wrapping obscures the barcode, preventing proper scanning. This is a Class III recall affecting the specific product distributed by Enovachem Pharmaceuticals. The recall applies to a single-use lidocaine injection product meant for prescription use only.
- Recalling firm
- Asclemed USA Inc.
- Product
- 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.
- Reason
- Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
- Classification
- Class III
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-07-15
- Status
- Ongoing
- Distribution
- Within U.S. - Tennessee
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/ca1d4cfd-0942-4fea-af91-ae89180f930d