Arthrex, Inc.: Medical Device Recalls in 2021

According to to data from the FDA, there were 3 medical device recalls made by Arthrex, Inc. in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

• Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
• Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
• Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and fractures of the proximal tibia and distal femur.