← FDA ENFORCEMENT
Z-1495-2026Class II

KOB GmbH

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
KOB GmbH
Product type
Device
Status
Ongoing
Report date
2026-03-18
Distribution
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
Firm state
N/A
Product quantity
35,328
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010

Code / lot info

Model/Catalog Number: NONUNNAS40 KOB article #40307010 Customer Code: (01)10888277675438 Lot Numbers: 2520206 2520739

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →