HIGHFDA DRUG

K Kirkman FIVE-STAR VASOCAINE Spray Recall for Expiry-Date Stability Issue (2026)

HTO Nevada Inc. dba Kirkman recalls 27,380 bottles of FIVE-STAR VASOCAINE Spray distributed nationwide by Dermal Source. The recall cites stability data that does not support the product's expiry date. Stop using the spray and contact Kirkman or your healthcare provider for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
February 18, 2026
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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
Topical anesthetic spray with lidocaine and vasoconstrictor (Lidocaine HCl 4%, Racepinephrine HCl 0.01%)
Model numbers
839CP-0016, 839CP-0017, 839CP-0018, 839CP-0019, 839CP-0020, 839CP-0021, 839CP-0022, 839CP-0023 +1 more
Sizes
4 oz
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    February 18, 2026

  2. Reported by FDA DRUG

    March 11, 2026

  3. RecallRadar source check

    March 18, 2026

  4. 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

FIVE-STAR VASOCAINE Spray is a topical anesthetic with lidocaine and a vasoconstrictor used for minor procedures.

Why This Is Dangerous

Stability data does not support the expiry date, raising concerns about potency or safety if used beyond expiry.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Consumers may face degraded effectiveness or safety concerns if using an expired or unstable product; no incidents are detailed in the notice.

Practical Guidance

How to identify if yours is affected

  1. Verify NDC 80069-016 on the product label.
  2. Review lot numbers 839CP-0016 through 839CP-0024 and corresponding expiry dates.
  3. Compare with recall notice.

Where to find product info

FDA enforcement page for recall D-0385-2026 and Kirkman notice

What timeline to expect

Refunds or replacements, if offered, are not specified in the notice.

If the manufacturer is unresponsive

  • Document all contact attempts with Kirkman.
  • File a complaint with the FDA if you suspect unsafe product handling or lack of remedy.

How to prevent similar issues

  • Always check expiry date before use.
  • Do not use products with unclear or missing expiry information.
  • Ask healthcare providers for current, in-date products.

Documentation advice

Keep the product packaging, recall notice, and any correspondence with Kirkman; take photos of label and lot numbers for records.

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Product Details

Brand: Kirkman (HTO Nevada Inc. dba Kirkman) Product: FIVE-STAR VASOCAINE Spray Active ingredients: Lidocaine HCl 4%, Racepinephrine HCl 0.01% Size: 4 oz bottles NDC: 80069-016 Distributed by: Dermal Source, Portland, OR 97232 Quantity recalled: 27,380 bottles Lot numbers and EXP dates: - 839CP-0016 — EXP 2026-03-31 - 839CP-0017 — EXP 2026-06-30 - 839CP-0018 — EXP 2026-08-31 - 839CP-0019 — EXP 2026-10-31 - 839CP-0020 — EXP 2027-03-31 - 839CP-0021 — EXP 2027-07-31 - 839CP-0022 — EXP 2027-11-30 - 839CP-0023 — EXP 2028-02-29 - 839CP-0024 — EXP 2028-07-31 Recall date: 2026-02-18 Status: Active Rem

Key Facts

  • Lot numbers 839CP-0016 to 839CP-0024
  • Exp dates range Mar 31, 2026 to Jul 31, 2028
  • Recall 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
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeTopical anesthetic spray with lidocaine and vasoconstrictor (Lidocaine HCl 4%, Racepinephrine HCl 0.01%)
Sold At
Unknown

Product Details

Brand
Model Numbers
839CP-0016
839CP-0017
839CP-0018
839CP-0019
839CP-0020
+4 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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