Recall Z-0980-2019— Stryker GmbH
Class II · Terminated
Class II FDA medical device recall by Stryker GmbH, initiated 2019-01-21, terminated 2020-04-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty. Reason: The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set..
- Recalling firm
- Stryker GmbH
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-01-21
- Terminated
- 2020-04-02
- Firm location
- Selzach, N/A, Switzerland
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.