Compress Device Centering Sleeve, Compress Device And Compress Device Short Anti-rotation Spindle, Anti-rotation Elliptical Spindle, And Compress Instrument Drill For Anti-rotation Pin (2018-12-13)
Recall Summary The Canadian health authority is recalling specific orthopedic surgical components used in compress device systems, including centering sleeves, anti-rotation spindles, and drill instruments. The recall is classified as Class I, meaning there is a potential serious adverse health consequence. These devices were distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-01-09
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/70d6033e-7880-4bc9-9a81-b53288fa0472