Wright Medical Technology, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0564-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

PRO-STIM 10cc INJECTABLE, Part Number 86SR0410

Product Classification:

Class II

Date Initiated: November 8, 2016

Date Posted: December 4, 2019

Recall Number: Z-0564-2020

Event ID: 84180

Reason for Recall:

The firm discovered a lack of adequate documentation confirming sterility on certain products.

Status: Terminated

Product Quantity: 19 units

Code Information:

Lot Number 1564697

Distribution Pattern:

US and Norway, Italy, Germany, France, South Africa, UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, Spain

Voluntary or Mandated:

Voluntary: Firm initiated