Urgent Field Safety Notice For Zenition 10, Zenition 30 By Philips Medical Systems Nederland B.v

Recall Summary Philips Medical Systems Nederland B.V. has issued an urgent safety notice for Zenition 10 and Zenition 30 medical devices distributed in Germany and the EU. This is a Class I recall, indicating a serious safety concern. The specific reason for the recall is not clearly stated in the available information provided.

Recalling firm

Urgent Field Safety Notice for Zenition 10, Zenition 30 by Philips Medical Systems Nederland B.V , Download_Veroeffentli

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for Zenition 10, Zenition 30 by Philips Medical Systems Nederland B

Reason

assessment Field corrective actions Urgent Field Safety Notice for Zenition 10, Zenition 30 by Philips Medical Systems Nederland B

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-05-05

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/72c5e945-32bd-47ef-82ba-7110fc07142a