Ortho Development recalls

Ortho Development appears in 8 official U.S. recall notices indexed by RecallRadar, most recently on 2020-05-13.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Tibial Tray Nonporous A Size 4
  FDA Device · Class II · 2020-05-13 · Ortho Development
• Tibial Tray Nonporous A Size 2
  FDA Device · Class II · 2020-05-13 · Ortho Development
• Patella 38mm, REF164-0038 Product Usage: UHMWPE component used in a TKA procedure to resurface the patella and serve as a bearing surface f…
  FDA Device · Class II · 2014-08-27 · Ortho Development
• PS Tibial Insert, REF 163-1XXX Product Usage: UHMWPE component used in TKA procedures to serve as a tibial bearing surface for articulation…
  FDA Device · Class II · 2014-08-27 · Ortho Development
• Tibila Insert CK, Balanced Knee System Revision, REF563-1YYY Product Usage: UHMWPE component used in TKA and revision TKA procedures to ser…
  FDA Device · Class II · 2014-08-27 · Ortho Development
• Pivot Bipolar Cup 22x42/43-51/53mm, REF 133-YYYY Product Usage: Used in a hemiarthroplasty procedure as the bearing surface to articulate w…
  FDA Device · Class II · 2014-08-27 · Ortho Development
• Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component used in TKA procedures to serve as a tibial bearing sur…
  FDA Device · Class II · 2014-08-27 · Ortho Development
• PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total kn…
  FDA Device · Class II · 2014-05-21 · Ortho Development