KOB GmbH recalls MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE
Reason for recall
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010Catalog # Number2 affected lots25202062520739
What the firm is doing
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
DistributionShow detailsHide
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- 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.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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