Stryker GmbH: Medical Device Recall in 2019 - (Recall #: Z-0980-2019)

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:

Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty

Product Classification:

Class II

Date Initiated: January 21, 2019

Date Posted: March 13, 2019

Recall Number: Z-0980-2019

Event ID: 82140

Reason for Recall:

The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.

Status: Terminated

Product Quantity: 17 units

Code Information:

Lot Number(s): K026ACE (lot# packaging) KU97181 (Vendor code engraved on device)

Distribution Pattern:

In the countries of Canada and Korea

Voluntary or Mandated:

Voluntary: Firm initiated