Ie33 Diagnostic Ultrasound System-sector Transducer And Epiq Ultrasound Transducers (2019-09-06)
Recall Summary Philips is recalling certain IE33 Diagnostic Ultrasound System sector transducers and EPIQ ultrasound transducers distributed across Canada due to a defect that could affect device performance. This recall affects healthcare facilities and medical providers using these ultrasound equipment models. The FDA classified this as a Class I recall, indicating the defect poses a serious risk to patient safety.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-09-20
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/25185e2f-5582-481d-aa44-8e941b097fd0