Philips Ct Areta/rembra Systems
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Philips CT Areta/Rembra systems. [Device]. Model: CT Rembra RT. Affected: CT Areta/Rembra software version 6.0.0.X
- Reason
- The manufacturer has identified multiple software issues in CT Areta/Rembra software version 6.0.0.X. These issues may result in reconstruction failures, scan interruptions, image artifacts, positioning inaccuracies, or corrupted images.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-09-07
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/fcd3ecfa-c13c-424b-970b-ea010bebf776