Stryker Autoplex System Without Needles And Cement (2016-06-13)
Stryker Autoplex System Recall Summary Stryker is recalling the Autoplex System without needles and cement across Canada due to safety concerns with this medical device. The specific details about what defect prompted the recall and which patients or healthcare settings are affected are not provided in the available information. This is classified as a Class I recall, which is the most serious type.
- 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/a7ca3b80-6947-43d5-975d-a573ac8c2a1b