Radiography 7000 M
Philips Medical Systems is recalling software for the Radiography 7000 M system used in hospitals and laboratories in New Zealand. The software needs to be upgraded as part of the recall action. This is classified as a Class I recall, which indicates a serious issue.
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Radiography 7000 M. [Device]. Model: Model number - 712010
- Reason
- The manufacturer has identified additional software problems that may impact clinical workflow., (1) Unintended Backward Movement: The manufacturer has become aware that the Radiography 7000 M system may continue to move a short distance after releasing the drive handle while reversing. This issue only occurs if the drive handle is released before the system comes to a full stop., (2) Detector Pairing Issue: When the Radiography 7000 M system clock is changed or restored (due to day light saving or after reinstalling software), there is a potential for the console user interface and tube...
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-06-10
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/bef3b2d4-a0ce-4474-8e45-cbbd7c15510e