[mdr] Spectral Ct, Iqon Spectral Ct, Brilliance Ict, Brilliannce Ict Upgrade

Recalling firm
Philips New Zealand Commercial Limited
Product
[MDR] Spectral CT, IQon Spectral CT, Brilliance iCT, Brilliannce iCT Upgrade. [Device]. Model: Product code: 738333 Spectral CT; Product code: 738333 Spectral CT. Affected: Software version - V5.0.x, V5.2.x, V5.4.x; Software version - V5.0.x, V5.2.x, V5.4.x. Also covers: BEST CT Systems
Reason
The manufacturer has identified 24 software issues that may affect certain Spectral CT systems. Affected customers will be contacted to arrange installation of the necessary software update to resolve these issues.
Classification
Class I
Category
medical device recall
Country
New Zealand
Agency
MEDSAFE
Recall date
2026-09-14
Status
Ongoing
Distribution
New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/d4975f1c-20c6-4ad5-a6f9-60234210279e