# FDA recall Z-0980-2019

> **Stryker GmbH** · Class II · device recall initiated 2019-01-21.

## 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

- **Recall number:** Z-0980-2019
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **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

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

## Citation

> AI Analytics. FDA recall Z-0980-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0980-2019. Source: US FDA. Licensed CC0.

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