Smith & Nephew, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2883-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis

Product Classification:

Class II

Date Initiated: August 1, 2017

Date Posted: August 29, 2018

Recall Number: Z-2883-2018

Event ID: 80752

Reason for Recall:

Two lots of Genesis II Non Porous C/R Femoral Size 6 right packaged were distributed containing Genesis II C/R Femoral Size 4 left.

Status: Terminated

Product Quantity: 27 units

Code Information:

Lot Numbers: 16CMB0061A, 16CMB0066A

Distribution Pattern:

Australia, Austria, Germany, Great Britain, Poland, Spain

Voluntary or Mandated:

Voluntary: Firm initiated