FDA Device recall Z-3263-2024
eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal
- FDA Device
- Class III
- ongoing
- Published 2024-10-02
On 2024-10-02 the FDA classified a Class III recall of eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal by T G Eakin, citing on lot of cartons of Eakin Cohesive small seals, Model Number 839002 may contain blistered seals labelled as 839005.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3263-2024 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2024-08-08 |
| Published | 2024-10-02 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | T G Eakin |
| Distribution | KY |
Product
eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal
Reason
On lot of cartons of Eakin Cohesive small seals, Model Number 839002 may contain blistered seals labelled as 839005.
Identifiers
| code_info | UDI/DI 00768455108732, Lot number 109357C553 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3263-2024%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.