Smartstitch Suturing Device - Perfectpasser Connector (2019-02-21)

SmartStitch Suturing Device Recall Summary The PerfectPasser Connector component of the SmartStitch Suturing Device is being recalled across Canada. The device has been classified as a Class I recall, which indicates a serious safety issue. This recall affects medical devices that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-03-08
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6ba73ba5-6951-44f0-957e-08f0715c5e6b