T.G. Eakin Limited: Device Recall

Recall #Z-3263-2024 · 08/08/2024

Class III: Low Risk

Recall Details

Recall Number
Z-3263-2024
Classification
Class III
Product Type
Device
Recalling Firm
T.G. Eakin Limited
Status
Ongoing
Date Initiated
08/08/2024
Location
Comber, Ireland
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
35,400 cartons of 20 individually packaged seals

Reason for Recall

On lot of cartons of Eakin Cohesive small seals, Model Number 839002 may contain blistered seals labelled as 839005.

Product Description

eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal

Distribution Pattern

US: KY

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.