Wolfstein, N/A, Germany
KOB GmbH recalls
1 recall recorded since 2018, most recently on 15 January 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 15 January 2026
- Reason
- Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
- Distribution
- U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1495-2026
- MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.