HIGH

Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)

Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

Quick Facts at a Glance

Recall Date
February 18, 2026
Hazard Level
HIGH
Brand
Kirkman
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Stability Data Does Not Support Expiry Date.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact HTO Nevada Inc. dba Kirkman or your healthcare provider for guidance. Notification method: E-Mail

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Product Details

Product: MAXIMUM Zone 1 4% Lidocaine Cream, 1/2 oz bottles. NDC: 80069-014. Lot #: 807CP-0003. Expiry date: 07/31/2026. Sold nationwide in the U.S. Distribution: Dermal Source, Portland, OR 97232. Quantity: 178 bottles.

The Hazard

The recall notes that stability data does not support the expiry date. Use of products past their expiry date could result in reduced potency or unsafe results.

What to Do

1. Stop using the product immediately. 2. Check the bottle for Lot #: 807CP-0003 and Expiry: 07/31/2026. 3. Contact HTO Nevada Inc. dba Kirkman via email for guidance. 4. If you have health concerns, consult a healthcare provider. 5. Follow Kirkman’s instructions for any refunds or replacements.

Contact Information

Recall information is available on the FDA enforcement page. Remedial guidance directs consumers to contact Kirkman by email. Official enforcement notice: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0386-2026. For detailed instructions, contact Kirkman via the recall notice.

Key Facts

  • 178 bottles recalled
  • Lot #: 807CP-0003
  • Exp. Date 07/31/2026
  • NDC 80069-014
  • Distributed nationwide in the U.S. by Dermal Source
  • Recall date 2026-02-18; status ACTIVE

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Brand
Model Numbers
Lot #: 807CP-0003
Exp. Date 07/31/2026.
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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