FDA recall Z-0980-2019

Stryker GmbH · Class II · device

Product

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

Reason for recall

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

Distribution

In the countries of Canada and Korea

Key facts

Status
Terminated
Initiation date
2019-01-21
Report date
2019-03-13
Termination date
2020-04-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Selzach, N/A, Switzerland

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0980-2019