D-0713-2026 Class III Ongoing
FDA drug recall D-0713-2026 was initiated by Asclemed USA Inc. on July 15, 2026 and is designated Class III. Reason for recall: Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan The recall status is ongoing. Affected quantity: 18 kits.
Recall Details
- Product Type
- Drugs
- Report Date
- July 29, 2026
- Initiation Date
- July 15, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18 kits
Product Description
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 for Recall
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Distribution Pattern
Within U.S. - Tennessee
Code Information
Lot: 070126X1, Exp. 12/31/2027.