MAXIMUM ZONE 2 Lidocaine Cream Recall
MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232
Updated February 18, 2026
MAXIMUM ZONE 2 4% Lidocaine Cream (containing lidocaine and epinephrine) is being recalled because stability testing does not support the listed expiry date. The product may lose potency or safety over time if used beyond its actual shelf life.
Is the HTO Nevada Inc. dba Kirkman recalled? Yes. This product was recalled by FDA on February 18, 2026. Details below.
What is recalled
MAXIMUM, ZONE 2, 4% Lidocaine Cream (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, NDC 80069-015, distributed by Dermal Source, Portland, OR 97232.
Am I affected
You're affected if you own a 1 oz bottle of MAXIMUM ZONE 2 4% Lidocaine Cream with NDC number 80069-015.
What to do right now
Stop using this product. Contact the manufacturer or the seller for instructions on return or disposal.
The hazard
Stability Data Does Not Support Expiry Date.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0387-2026
- Classification
- Class II
- Recalled
- February 18, 2026
Get free recall alerts
New Drugs & Medications recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.
More Drugs & Medications recalls
BD ChloraPrep Hi-Lite Orange Recall
BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic) were distributed without proper sterilization assurance. These products should have been sterilized …
CareFusion 213, LLC
Methohexital Sodium Injection Recall
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
ONESOURCE SPECIALTY PHARMA LIMITED
Lacosamide Tablets 100mg Recall
Lacosamide 100mg tablets made by Camber Pharmaceuticals may contain a different medication, Selexipag 1000 mcg, mixed into the bottle. Taking the wrong drug by …
Annora Pharma Private Limited