3dicrosscheck Lap 0 Left Ortholoc 3di Plating System (2019-09-26)

Recall Summary The 3DiCROSSCHECK LAP 0 LEFT ORTHOLOC 3DI PLATING SYSTEM has been recalled across Canada due to issues with this medical device. The device is used for orthopedic surgical procedures. This is classified as a Class I recall, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-10-11

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/074c5f9e-1a90-4d0b-8ecf-aeef2f15da23