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.