Z-0139-2023 Class II Terminated
FDA device recall Z-0139-2023 was initiated by Wright Medical Technology, Inc. on Sep 30, 2022 and is designated Class II. Reason for recall: The tibial tray lock detail is oversized (larger than specification). The recall status is terminated (terminated Aug 21, 2026). Affected quantity: 1 unit.
Recall Details
- Product Type
- Devices
- Report Date
- Nov 2, 2022
- Initiation Date
- Sep 30, 2022
- Termination Date
- Aug 21, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Product Description
Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Reason for Recall
The tibial tray lock detail is oversized (larger than specification).
Distribution Pattern
US Nationwide distribution in the state of New York.
Code Information
GTIN 00840420124142, Lot Code: 1726308
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0139-2023
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026