Blue Belt Technologies MN: Medical Device Recalls in 2014
Updated on March 25, 2026.
According to to data from the FDA, there were 3 medical device recalls made by Blue Belt Technologies MN in 2014. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
- Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
- Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.