Epiq 5 And 7 Ultrasound Systems (2016-03-22)
EPIQ 5 and 7 Ultrasound Systems Recall Philips is recalling EPIQ 5 and 7 ultrasound systems distributed across Canada due to a defect in the medical device. This recall is classified as Class I, meaning there is a serious risk of adverse health effects. The recall affects ultrasound systems that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-04-04
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/22edf0cc-4f17-416b-b7b6-87e0548d05ae