Warning
HTO Nevada Inc. dba Kirkman Recalls MAXIMUM
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0386-2026Drug / Pharmaceutical
HTO Nevada Inc. dba Kirkman Recalls MAXIMUM
HTO Nevada Inc. dba Kirkman · Class II — Moderate Risk
Product Description
MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.
Reason for Recall
Stability Data Does Not Support Expiry Date.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Nationwide within the U.S
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
Sources: FDA openFDA Enforcement Database