Devices

Device Recall UCPLUS Solution

Model / Serial
26014: Lot number 0305.13.2814, 26016: Lot number 0305.13.2815, 26018: Lot number 0305.13.2816, 26020: Lot number 0305.13.2817 Serial Number: None
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
California
Product Description
UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26014 Femoral Component Size 4, 26016 Femoral Component Size 6, 26018 Femoral Component Size 8 and 26020 Femoral Component Size 10
Manufacturer
Plus Orthopedics USA
1 Event
- Recall of Device Recall UCPLUS Solution

Manufacturer

Plus Orthopedics USA

Manufacturer Address
Plus Orthopedics USA, 10188 Telesis Ct, San Diego CA 92121-4779
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall UCPLUS Solution

Model / Serial
Lot Number: All lots considered affected Serial Number: None
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
California
Product Description
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
Manufacturer
Plus Orthopedics USA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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