Urgent Field Safety Notice For Philips Allura And Azurion Systems By Philips Medical Systems Internatonal Bv

Recall Summary Philips Medical Systems is issuing an urgent field safety notice for Philips Allura and Azurion systems, which are medical imaging devices used in hospitals and clinical settings. The notice affects devices distributed in Germany and the EU. The specific reason for the recall was not clearly stated in the available information, but it has been classified as a Class I safety issue, which is the most serious classification level.

Recalling firm

Urgent Field Safety Notice for Philips Allura and Azurion systems by Philips Medical Systems Internatonal BV , Download_

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for Philips Allura and Azurion systems by Philips Medical Systems Internatonal BV 2026

Reason

assessment Field corrective actions Urgent Field Safety Notice for Philips Allura and Azurion systems by Philips Medical Systems Internatonal BV 2026

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-05-15

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/845c41ad-6f5b-4f20-a579-123441467c43