Compress Device Centering Sleeve, Anti-rotation Spindle, Anti-rotation Elliptical Spindle, And Compress Instrument Drill For Anti-rotation Pin (2018-10-22)

Recall Summary Several compression device components (centering sleeve, anti-rotation spindles, and drill instrument) are being recalled across Canada due to issues with the medical devices themselves. This is a Class I recall, which is the most serious classification. The affected products were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-11-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5d7b3c72-4c57-476c-bed3-7bb0e3529259