Smith & Nephew, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1507-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

Product Classification:

Class II

Date Initiated: December 19, 2019

Date Posted: March 25, 2020

Recall Number: Z-1507-2020

Event ID: 84647

Reason for Recall:

LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part

Status: Terminated

Product Quantity: 29 units

Code Information:

Lot Number 19FM12500; Product Number 71453221.

Distribution Pattern:

USA: TN, NC, CA,OR, NM, TX, PA, MI, LA, DA, IL. Int'l: IT (Italy), NL (Netherlands), RO (Romania), PR (Puerto Rico).

Voluntary or Mandated:

Voluntary: Firm initiated