Is this bandage still safe to use if it looks fine?

No. The recall is due to labeling omissions. Stop using the product and consult the manufacturer for steps.

What should I do with affected units?

Do not use them. Follow the recall instructions and contact KOB GmbH for guidance.

Where can I verify if my lot is affected?

Check the recall page or contact the manufacturer with the article and lot numbers.

Will I get a refund or replacement?

The recall notice instructs to follow the manufacturer for remedies, typically refunds or replacements are offered.

What identifiers help me verify if my product is affected?

Model NONUNNAS40, KOB article #40307010, lot numbers 2520206 and 2520739.

Who issues the recall?

KOB GmbH with notification by letter; product classified as Class II recall.

What is the exact defect?

Labeling incomplete. Missing ingredients castor oil and calamine on the label.

What jurisdictions are involved?

U.S. distribution in Illinois with other U.S. distribution not fully detailed; product manufactured outside the U.S.

How urgent is the recall?

High risk due to labeling inaccuracies that could affect safe use.

How do I contact for more information?

Refer to the FDA recall page linked in the notice.

Will there be more updates?

The status is ACTIVE; follow the manufacturer and FDA updates.

HIGHJanuary 15, 2026

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.

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

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

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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

Locate model NONUNNAS40 and KOB article #40307010 on the device label
Check lot numbers 2520206 or 2520739
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

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
Recall date: 2026-01-15
Model/Catalog Number: NONUNNAS40 KOB article #40307010
Lot Numbers: 2520206, 2520739
Countries: United States (IL); Manufactured outside the U.S. (O.U.S.)

View Original Recall on FDA - Medical Devices

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Safety Assessment

Risk LevelHIGH

Severity Score

8/ 10

Affected Groups

GENERALPREGNANTPETS

Injury Types

LACERATIONOTHER

Product Classification

CategoryHealth & Personal Care › Medical Devices

Product TypeBandage (Zinc Paste)

Product Details

Jul 25, 2025

Medline

Medline Industries,