Asclemed USA Inc. recalls Lidolog Kit
- Recalling company
- 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 – not likely to cause adverse health consequences
- Recall date
- Jul 15, 2026
- Reported
- Jul 29, 2026
- Distribution
- Within U.S. - Tennessee
- Status
- Ongoing
- Quantity
- 18 kits
- Lot / codes
- Lot: 070126X1, Exp. 12/31/2027.
- Company location
- Torrance, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0713-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0713-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.