Urgent Field Safety Notice For Gundry Oder Dlp Kanülen By Medtronic Inc

Recall Summary Medtronic Inc is issuing an urgent safety notice for Gundry and DLP cannulas distributed in Germany and the EU. This is a Class I recall, which indicates a serious issue with the devices. The specific reason for the recall is not detailed in the provided information.

Recalling firm

Medtronic Inc

Product

Gundry oder DLP Kanülen

Reason

Urgent Field Safety Notice for Gundry oder DLP Kanülen by Medtronic Inc

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-04-24

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/e91a095d-00ef-483b-93db-a173a790b4f5