Philips Duradiagnost X-ray System (2016-06-22)
Philips DuraDiagnost X-ray System Recall Philips is recalling DuraDiagnost X-ray systems distributed across Canada due to a medical device issue. The FDA classified this as a Class I recall, indicating a serious safety concern. The recall affects X-ray equipment that may have been installed in medical facilities.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-07-19
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/62cdbbc5-60a8-4e8f-b64d-f1ac6182a3e0