Plus Orthopedics USA UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26004 Femoral Component Size 4, 26006 Femoral Component Size 6, 26008 Femoral Component Size 8 and 26010 Femoral Component Size 10 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26004 Femoral Component Size 4, 26006 Femoral Component Size 6, 26008 Femoral Component Size 8 and 26010 Femoral Component Size 10
Brand
Plus Orthopedics USA
Lot Codes / Batch Numbers
Lot Number: All lots considered affected Serial Number: None
Products Sold
Lot Number: All lots considered affected Serial Number: None
Plus Orthopedics USA is recalling UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26004 Femoral Component Size 4, 26006 Fem due to There exists the possibility that incomplete bony support or insufficient cementing of the implanted device can result in fatigue fracture of the UC-P. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There exists the possibility that incomplete bony support or insufficient cementing of the implanted device can result in fatigue fracture of the UC-PLUS Solution Femoral Component.
Recommended Action
Per FDA guidance
The depth of the withdrawal action taken in June, 2003 was to the distributor (agent) level. Plus USA contacted individual agent sites showing inventory of the affected article numbers on hand and requested that those items be returned to Plus USA.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA
Page updated: Jan 10, 2026