FDA recall: HTO Nevada Inc. dba Kirkman — MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Sour (Feb 18, 2026)

HTO Nevada's MAXIMUM 4% lidocaine cream (distributed by Dermal Sour) is recalled. This is a compounded or private-label topical anesthetic commonly used in aesthetic practices for pre-procedure numbing. A recall on a lidocaine cream signals potential issues with sterility, potency, or formulation stability — all critical for patient safety and treatment efficacy. If you're using this product for pre-injection or pre-laser prep, stop immediately and audit your stock. Contact your supplier to confirm whether your lot is affected and arrange replacement. Switch to a cleared, branded alternative in the interim. Document the recall and your response in your compliance file. Check the FDA enforcement page for lot numbers and distribution details.