US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 9, 2023 (4 years ago)

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

What was recalled

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure, distributed by: DERMAL SOURCE, Portland, OR, www.dermalsource.com, 1-866-568-3223, NDC code: 80069-012-01, Drug Facts- For use by licensed professionals only' Active Ingredients- Lidocaine HCL (5%), Epinephrine (0.01%).

Recalling firm
HTO Nevada, Inc.
Origin
OR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0271-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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