Various Guide Wire Products From Zimmer Inc. (2018-04-05)

Guide Wire Recall Summary Zimmer Inc. is recalling various Guide Wire products that were distributed across Canada due to issues with these medical devices. This is classified as a Class I recall, which is the most serious type. The recall affects Guide Wire products from Zimmer Inc. that were in use or distribution throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-04-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/50ec0594-08fe-45fd-87f0-60a7fad4f7bc