Wright Medical Technology, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2797-2020)

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:

Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wires to assist in removal of cannulated screws. This product is a multiple use, non-sterile instrument.

Product Classification:

Class II

Date Initiated: July 28, 2020

Date Posted: August 19, 2020

Recall Number: Z-2797-2020

Event ID: 85982

Reason for Recall:

Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.

Status: Terminated

Product Quantity: 9 units

Code Information:

product is not lot coded

Distribution Pattern:

US Nationwide distribution including in the states of CO, TX, OR, KX, SC, CA, AR, NJ, UT, VA, MO, NC, FL, IL.

Voluntary or Mandated:

Voluntary: Firm initiated