DeviceSignal · Recall classified

United Orthopedic Corp.

FDA classified a device recall on 2026-08-05 · Class II · Z-2885-2026

EventRecall classified
Effective2026-08-05
ClassificationClass II

On 2026-08-05 the FDA classified a device recall from United Orthopedic Corp. as Class II. Product: Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right…. Recall Z-2885-2026. The firm initiated it on 2026-05-20. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-2885-2026
Classification
Class II
Classified on
2026-08-05
Initiated on
2026-05-20
Firm
United Orthopedic Corp.
Reason
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Product
Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right Model/Catalog Number: 9323-5333 and 9323-5334 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No

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-2885-2026
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
4d64083905a0f438f2ca916552c4934a082eb2b594362723afba937df1a35f17
Signal type
device_recall.classified

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)