Arthrex, Inc.: Medical Device Recalls in 2017

According to to data from the FDA, there were 7 medical device recalls made by Arthrex, Inc. in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
• Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching
• Anthrex PEEK SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching
• Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
• iBalance(R) UKA, Femoral Cemented, Size 3, Left Medial/Right LATERAL, REF AR 501-UFLC, QTY 1, Rx ONLY, STERILE R, Arthrex, Inc., Naples, FL Indicated for use in uni-compartmental knee arthroplasty as a result of: 1. Moderately disabling joint disease of the knee resulting from painful osteoarthritis or posttraumatic arthritis. 2. Correction of functional deformity. 3. Revision of previous unsuccessful uni-compartmental knee replacement or other procedure. 4. As an alternative to tibial osteotomy in patients with uni-compartmental osteoarthritis.
• Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching
• Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm