FDA Drugs recall ·
Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial… recall
- Recall number
- D-0713-2026
- Date
- (initiated July 15, 2026)
- Company / brand
- Asclemed USA Inc.
379 Van Ness Ave Ste 1403, Torrance, CA, United States - Category
- Drugs › Class III
- Classification
- Class III
- Status
- Ongoing
- Units affected
- 18 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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.
Why was it recalled?
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot: 070126X1, Exp. 12/31/2027.
Distribution
Within U.S. - Tennessee
States: Tennessee
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (drugs), recall D-0713-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.