Urgent Field Safety Notice For Sphere 9 Katheter By Medtronic Inc

Recall Summary Medtronic Inc. is issuing an urgent safety notice for the SPHERE 9 Katheter, a medical device distributed in Germany and the EU. The company has classified this as a Class I safety issue, which is the most serious classification. The notice does not specify the particular safety concern or which patients may be affected.

Recalling firm

Medtronic Inc

Product

SPHERE 9 Katheter

Reason

Urgent Field Safety Notice for SPHERE 9 Katheter by Medtronic Inc

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-03-31

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/d499eb60-f734-4aad-a907-c786a4e9def8