DeviceSignal · Recall classified
United Orthopedic Corp.
FDA classified a device recall on 2026-08-06 · Class II · Z-2898-2026
EventRecall classified
Effective2026-08-06
ClassificationClass II
On 2026-08-06 the FDA classified a device recall from United Orthopedic Corp. as Class II. Product: Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 2mm and 6mm…. Recall Z-2898-2026. The firm initiated it on 2026-03-19. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2898-2026
- Classification
- Class II
- Classified on
- 2026-08-06
- Initiated on
- 2026-03-19
- Firm
- United Orthopedic Corp.
- Reason
- Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
- Product
- Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 2mm and 6mm Model/Catalog Number: 9323-5312 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2898-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
24f51003b5cd447feccb435e644416081e83bccaf9b53f69aaf61266137bf9f8- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)