Spectral Ct, Iqon Spectral Ct, Brilliance Ict, Brilliannce Ict Upgrade
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Spectral CT, IQon Spectral CT, Brilliance iCT, Brilliannce iCT Upgrade. [Device]. Model: Spectral CT; Philips Spectral CT 7500 systems. Affected: Product code 728333; Product code 728333. Also covers: Philips Spectral CT 7500 Systems
- Reason
- The affected cables supply power from the Power Supply Unit to the DCDC board and then to the Detector Measurement System. Due to insufficient crimping, the cable connections can develop increased electrical resistance, which may lead to system failures and render the unit unusable until repairs are completed., During a scan, this issue may cause the scan to stop unexpectedly, generate the error code S_DMC_MODULE_VOLTAGE_OUT_OF_SPEC, or produce degraded image quality or image artifacts. In some cases, a patient re-scan may be required.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-03-20
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/33157590-a75d-4508-9473-0488edde909f