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KOB GmbH Unna-Z Stretch Zinc Paste Bandage Recall for Labeling Error

Medline Unna-Z Stretch Zinc Paste Bandage faces a high-risk labeling error. The recall covers 35,328 units distributed in the U.S. and other regions. Manufacturers warn to stop use immediately and follow recall instructions.

Official notice
KOBMedlineHealth & Personal CareMedical DevicesNONUNNAS40 KOB article #40307010

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 15, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
January 15, 2026
Hazard Level
HIGH
Brands
KOB, Medline
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

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 - Medical Devices; 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
KOB, Medline
Product type
Bandage (Zinc Paste)
Model numbers
NONUNNAS40 KOB article #40307010
Sold at
Unknown
Where affected
IL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 15, 2026

  2. Reported by FDA DEVICE

    March 18, 2026

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact KOB GmbH or your healthcare provider for instructions. Notification method: Letter

About This Product

Unna-Z Stretch Zinc Paste Bandage is used to protect and cover wounds and provide a zinc-based barrier in medical care.

Why This Is Dangerous

Incomplete labeling could mislead users about ingredients, potentially causing adverse reactions for those with allergies or sensitivities.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using affected bandages and await instructions; no injuries reported in the provided data.

Practical Guidance

How to identify if yours is affected

  1. Locate model NONUNNAS40 and KOB article #40307010 on the device label
  2. Check lot numbers 2520206 or 2520739
  3. Confirm U.S. distribution in IL or check if other U.S. locations were affected

Where to find product info

FDA recall page and manufacturer communications; look for recall number Z-1495-2026

What timeline to expect

Refunds or replacements handled by the manufacturer; timeline not specified

If the manufacturer is unresponsive

  • File a complaint with the FDA
  • Contact consumer protection offices
  • Keep all correspondences and photos of the label for records

How to prevent similar issues

  • Always verify labeling for complete ingredient lists
  • Consult healthcare professionals before applying products containing castor oil or calamine if allergies exist
  • Purchase from reputable suppliers with recall monitoring

Documentation advice

Retain product, photos of label, recall notice, and all communications

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Product Details

Product: MEDLINE UNNA-Z Stretch Zinc Paste Bandage, Ref NONUNNAS40, KOB article #40307010. Class II recall. Quantity: 35,328 units. Recall date: 2026-01-15. Distribution: U.S. - Illinois; Other U.S. states not provided; Manufactured outside the U.S. (O.U.S.). Brand: KOB GmbH.

Reported Incidents

No specific injuries or incidents are reported in the provided data.

Key Facts

  • Quantity: 35,328 units recalled
  • Model/Catalog Number: NONUNNAS40 KOB article #40307010
  • Countries: United States (IL); Manufactured outside the U.S. (O.U.S.)

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
GENERALPREGNANTPETS
Injury Types
LACERATIONOTHER

Product Details

Model Numbers
NONUNNAS40 KOB article #40307010
Affected States
IL
Report Date
March 18, 2026
Recall Status
ACTIVE

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