FDAFDA recall D-0713-2026 · Jul 29, 2026
Asclemed USA Inc.: Lidolog Kit recall
Recall found
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 for recall
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class III: use of or exposure to the product is not likely to cause health problems.
- Status
- Ongoing
- Codes, lots and dates
- Lot: 070126X1, Exp. 12/31/2027.
- Quantity
- 18 kits
- Distribution
- Within U.S. - Tennessee
- Recalling firm
- Asclemed USA Inc., Torrance, CA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-15
Source: openFDA enforcement record D-0713-2026 · search recall number D-0713-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 31, 2026, 6:32 AM EDT. The agency notice is the final word.