Pipeline Flex Embolization Device And Pipeline Flex Embolization Device With Shield Technology (2020-02-18)
Recall Summary Medtronic is recalling Pipeline Flex Embolization Devices and Pipeline Flex Embolization Devices With Shield Technology across Canada due to a manufacturing defect that could cause the device to separate or fracture during use. These devices are used to treat certain brain aneurysms through minimally invasive surgery. The recall affects medical facilities and patients who received these devices.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-03-03
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/da4bba50-f276-4a68-a031-e864be92c423