FDA Medical devices recall ·
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE recall
- Recall number
- Z-1495-2026
- Date
- (initiated January 15, 2026)
- Company / brand
- KOB GmbH
Lauterstr. 50, Wolfstein, N/A, Germany - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 35,328
- Hazard tags
- Mislabeling
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
Why was it recalled?
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model/Catalog Number: NONUNNAS40 KOB article #40307010 Customer Code: (01)10888277675438 Lot Numbers: 2520206 2520739
Distribution
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
States: Illinois
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1495-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.