OVERLOOKED

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Class IIIOngoing

Asclemed USA Inc. recalls Lidolog Kit

Recall date · record updated Jul 29, 2026 · Source: U.S. Food and Drug Administration (openFDA drug enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Asclemed USA Inc.
Reason
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Hazard
FDA Class III: not likely to cause adverse health consequences (FDA definition).
Who’s affected
Within U.S. - Tennessee
Where
Tennessee
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99408…

Products

  1. 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.

    Codes/lots: Lot: 070126X1, Exp. 12/31/2027.Quantity: 18 kitsRecall no. D-0713-2026Class III

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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