Class II — KOB GmbH
| Recalling firm | KOB GmbH |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine. |
| Product | MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010 |
| Quantity | 35,328 |
| Distribution | U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S. |
| Initiated | 2026-01-15 |
| Classified | 2026-03-06 |
| Recall number | Z-1495-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — KOB GmbH (Z-1495-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98328/
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