Stryker GmbH: Medical Device Recall in 2020 - (Recall #: Z-0780-2020)

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:

Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050

Product Classification:

Class II

Date Initiated: December 5, 2019

Date Posted: January 15, 2020

Recall Number: Z-0780-2020

Event ID: 84458

Reason for Recall:

Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal.

Status: Terminated

Product Quantity: 433 (289 units U.S. / 144 units OUS)

Code Information:

All lots UDI: (01)07613327350210

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and countries of Switzerland, France, Spain, United Kingdom, Italy, Sweden, Netherlands, Australia.

Voluntary or Mandated:

Voluntary: Firm initiated