Recall Z-1495-2026— KOB GmbH
Class II · Ongoing
Class II FDA medical device recall by KOB GmbH, initiated 2026-01-15. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010. Reason: Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine..
- Recalling firm
- KOB GmbH
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-01-15
- Firm location
- Wolfstein, N/A, Germany
Product description
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
Reason for recall
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Data sourced from openFDA. This site is unofficial and independent of the FDA.