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Stryker GmbH recalls Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Recalled March 13, 2019 · FDA recall Z-0980-2019 · Stryker
Hazard
The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set. · FDA Class II
Units
17 units
Sold at
In the countries of Canada and Korea
Description
The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.
Product
Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →