O-arm 1000 Imaging System - Base Oarm (2016-07-19)
Recall Summary The O-ARM 1000 Imaging System Base OARM is being recalled across Canada due to safety concerns with this medical device. This recall affects healthcare facilities and hospitals that use this imaging equipment. The recall is classified as Class I, meaning there is a serious risk of adverse health consequences.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-08-10
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5e67d0d5-b13b-436b-a88a-88a50c98cc7b