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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Kirkman
- Product type
- Lidocaine Cream
- Model numbers
- Lot #: 807CP-0003, Exp. Date 07/31/2026.
- Sizes
- 1/2 oz
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 18, 2026
Reported by FDA DRUG
March 11, 2026
RecallRadar source check
March 18, 2026
Consumer action
Use the official remedy and keep documentation.
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
About This Product
MAXIMUM Zone 1 4% Lidocaine Cream is a topical anesthetic intended for minor skin procedures or analgesia in adults. Packaged in 1/2 oz bottles.
Why This Is Dangerous
Stability data does not support the expiry date. Using expired lidocaine cream may result in reduced potency or unsafe outcomes.
Industry Context
This recall is not described as part of a broader industry pattern.
Real-World Impact
Consumers may experience reduced effectiveness or unknown safety risk if used past expiry date. Immediate suspension of use is advised.
Practical Guidance
How to identify if yours is affected
- Check bottle label for Lot #: 807CP-0003.
- Check Expiry date: 07/31/2026.
- Verify distributor: Dermal Source on packaging.
Where to find product info
Recall details available at the FDA enforcement report for D-0386-2026.
What timeline to expect
Not specified in the recall notice.
If the manufacturer is unresponsive
- Document contact attempts to Kirkman by email
- Consider reporting to health authorities if safety concerns persist
How to prevent similar issues
- Check expiry dates before using any topical medication.
- Buy from reputable distributors and verify lot numbers.
- Keep medication out of reach of children.
Documentation advice
Keep the bottle, packaging, and recall notice. Save email communications with Kirkman.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
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.
Key Facts
- Distributed nationwide in the U.S. by Dermal Source
- Recall date 2026-02-18; status ACTIVE
Browse More Recalls
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.
