KOB GmbH recalls MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE

Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.

On 01/15/2026, the firm sent a "Medical Device Recall" letter to its distributor informing them that product is being recalled due to a labeling error. The product box/package contained an incomplete ingredient statement. The ingredients castor oil and calamine were missing from the product labeling. On 02/08/2026, the firm sent an updated "URGENT Medical Device Recall" Letter. Customers are instructed to: The products of the concerned lots must be scrapped. They shall not be used, distributed or made available on the market. For questions or assistance - use email simone.viering@kob.de

• FDA enforcement recordOfficial FDA database entry for Z-1495-2026
• FDA device classification · ITGOfficial FDA classification for this device type
• CFR regulation · 21 CFR 890.3025The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find KOB GmbHSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.