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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

Medline Unna-Z Zinc Paste Bandage Recalled for Incomplete Ingredient Labeling

Agency Publication Date: March 6, 2026
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Summary

KOB GmbH has recalled approximately 35,328 units of Medline Unna-Z Stretch Zinc Paste Bandages (model NONUNNAS40) because the product labels did not list all ingredients. Specifically, the labels failed to mention the presence of castor oil and calamine. The bandages were distributed in Illinois and manufactured in Germany.

Risk

The omission of castor oil and calamine from the ingredient list poses a risk to patients with sensitivities or allergies to these substances, as they may unknowingly use a product that could cause an adverse skin reaction or allergic response.

What You Should Do

  1. Check your bandage packaging for Medline Unna-Z Stretch Zinc Paste Bandage with model number NONUNNAS40 and lot numbers 2520206 or 2520739.
  2. Stop using the product. Return it to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or the manufacturer for further instructions.
  3. If you have questions regarding this recall, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE
Model / REF:
NONUNNAS40
40307010
Lot Numbers:
2520206
2520739
UDI:
10888277675438

Recall #: Z-1495-2026; KOB article #40307010

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98328
Status: Active
Manufacturer: KOB GmbH
Sold By: Medical distributors; Healthcare facilities
Manufactured In: Germany
Units Affected: 35,328
Distributed To: Illinois

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.