Lower risk Drug recall · FDA · Published February 18, 2026

Kirkman VasoCaine Spray Recall: Stability Issues May Affect Safety

Kirkman recalls VasoCaine spray bottles with stability issues that could affect safety. Check product labels for lot numbers and expiration dates to determine if your item is affected.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0385-2026Drug Kirkman ›

Lower-risk recall

Stability Data Does Not Support Expiry Date.

Take action

Contact the company

Recalling firmHTO Nevada Inc. dba Kirkman6400 Rosewood St · Lake Oswego, OR 97035-5392

✎ GovInfoNow plain-language explainer

Kirkman is recalling VasoCaine spray bottles due to stability problems that may make the product unsafe after its expiration date. This recall affects specific lot numbers and expiration dates. Read more at govinfonow.com/recall/31476-kirkman-vasocaine-spray-recall-stability-issues-may-affect-safety.

Source Summary by GovInfoNow · govinfonow.com/recall/31476-kirkman-vasocaine-spray-recall-stability-issues-may-affect-safety · Updated August 17, 2026 · FDA enforcement record: FDA #D-0385-2026

Cite this page

“Kirkman VasoCaine Spray Recall: Stability Issues May Affect Safety.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31476-kirkman-vasocaine-spray-recall-stability-issues-may-affect-safety. Based on FDA recall #D-0385-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0385-2026%22&limit=1).

HTO Nevada Inc. dba Kirkman recalled FIVE-STAR, VASOCAINE Spray distributed by Dermal Source due to stability data not supporting the expiry date, the FDA said on Feb. 18, 2026.

How to tell if you have it

Brand: Kirkman
Product: FIVE-STAR, VASOCAINE Spray (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles
Distributed By: Dermal Source, Portland, OR 97232
NDC: 80069-016
Lot #: 839CP-0016 through 839CP-0024
Exp. Dates: 03/31/2026, 06/30/2026, 08/31/2026, 10/31/2026, 03/31/2027, 07/31/2027, 11/30/2027, 02/29/2028, 07/31/2028
Units affected: 27,380 bottles

The hazard

The recall is classified as Class II because stability data does not support the listed expiry dates for the recalled lots.

Context

GovInfoNow's records show HTO Nevada Inc DBA Kirkman has one other recall on record since March 12, 2024. Other recent recalls of similar products include Safecor Health Fluphenazine Elixir Recall (Aug. 13, 2026), American Regent Epinephrine Injection Recall (Aug. 11, 2026), and Blaine Labs Recalls Antifungal Solution Due to Stability Testing Issues (April 8, 2026).

How to tell if you have this one

Check the product label for the lot number (839CP-0016 to 839CP-0024) and expiration date (March 31, 2026 through February 29, 2028). The product is distributed by Dermal Source in Portland, OR.

Brand
Kirkman
Category
Drug

FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Nationwide within the U.S

Recall number	Product, codes & lots	Quantity
D-0385-2026	FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.; Lot #: 839CP-0016, Exp. Date 03/31/2026; 839CP-0017, Exp. Date 06/30/2026; 839CP-0018, Exp. Date 08/31/2026; 839CP-0019, Exp. Date 10/31/2026; 839CP-0020, Exp. Date 03/31/2027; 839CP-0021, Exp. Date 07/31/2027; 839CP-0022, Exp.Date 11/30/2027; 839CP-0023, Exp. Date 02/29/2028; 839CP-0024, Exp. Date 07/31/2028.	27,380 bottles.
D-0386-2026	MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.; Lot #: 807CP-0003, Exp. Date 07/31/2026.	178 bottles
D-0387-2026	MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.; Lot #: 795CP-0005, Exp. Date 06/30/2026	243 bottles

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the lot number (839CP-0016 to 839CP-0024) and expiration date on the spray bottle.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide within the U.S” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 21 days after the firm started it.

Feb 18, 2026Firm started the recall
Mar 5, 2026FDA classified it Class II
Mar 11, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/31476-kirkman-vasocaine-spray-recall-stability-issues-may-affect-safety">Kirkman VasoCaine Spray Recall: Stability Issues May Affect Safety (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0385-2026 (February 18, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0385-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.