Wright Medical Technology, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1101-2020)

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:

WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220

Product Classification:

Class II

Date Initiated: December 27, 2019

Date Posted: February 12, 2020

Recall Number: Z-1101-2020

Event ID: 84673

Reason for Recall:

Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affected product.

Status: Terminated

Product Quantity: 39 devices

Code Information:

Lot Code 1633010

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated