Lfit Cocr V40 And Cocr Lfit Femoral Heads

Recall Summary LFIT COCR V40 and COCR LFIT femoral heads (components used in hip replacement surgery) are being recalled across Canada due to potential manufacturing defects that could affect their performance. These products may fail prematurely, requiring additional surgery for patients who received them. The recall affects hip replacement patients in Canada who received these specific femoral head components.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e5f70c6e-1d0c-49eb-a321-2fd66180b2a4