FDAFDA · Food and drugs·Recall number Z-0980-2019
Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Published March 13, 2019 · Recall initiated: January 21, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker GmbH
- Distributor
- In the countries of Canada and Korea
- Lot
- Lot Number(s): K026ACE (lot# packaging) KU97181 (Vendor code engraved on device)
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Switzerland
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