FDA Device recall Z-1495-2026
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
- FDA Device
- Class II
- ongoing
- Published 2026-03-18
On 2026-03-18 the FDA classified a Class II recall of MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010 by Kob, citing due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1495-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-01-15 |
| Published | 2026-03-18 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Kob |
| Distribution | IL |
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.
Identifiers
| code_info | Model/Catalog Number: NONUNNAS40 KOB article #40307010 Customer Code: (01)10888277675438 Lot Numbers: 2520206 2520739 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1495-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.