[mdr] Azurion

Recalling firm

Philips New Zealand Commercial Limited

Product

[MDR] Azurion. [Device]

Reason

Potential loss of imaging (X-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data which may result in a delay or termination of procedure and/or procedural complications

Classification

Class I

Category

medical device recall

Country

New Zealand

Agency

MEDSAFE

Recall date

2026-02-16

Status

Ongoing

Distribution

New Zealand

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/9b04195e-04db-4592-a92f-861ca5d59f81