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

Recall date

January 21, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0980-2019

FDA classification

Class II

Brand / firm

Stryker GmbH

Sold / distributed

In the countries of Canada and Korea

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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