Valleylab Laparoscopic Products (2016-07-08)

Valleylab Laparoscopic Products Recall Summary Valleylab laparoscopic surgical devices were recalled across Canada due to safety concerns with the medical devices themselves. This Class I recall affects healthcare facilities and surgical centers that use these products. The devices were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-07-22
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3a3cb4d3-cd7c-44bc-b954-6f90c45ef832