Smith & Nephew, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2163-2018)

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:

smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)

Product Classification:

Class II

Date Initiated: May 4, 2018

Date Posted: June 20, 2018

Recall Number: Z-2163-2018

Event ID: 80125

Reason for Recall:

One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification.

Status: Terminated

Product Quantity: 5 units

Code Information:

15FM16181

Distribution Pattern:

International only: United Arab Emirates, Spain, Mexico

Voluntary or Mandated:

Voluntary: Firm initiated