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Ortho Development Corporation Recalls

3 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Ortho Development Corporation.

3Total Recalls
0Critical
41Units Affected
May 30, 2019Most Recent
All Recalls

Every Ortho Development Corporation Recall

Sorted by most recent. Click any recall for full details.

3 recalls
High RiskFDA
Ortho Development Corporation
Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.
Medical Devices·27 affected·May 30, 2019
High RiskFDA
Ortho Development Corporation
Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component used in TKA procedures to serve as a tibial beari...
Medical Devices·13 affected·Jul 11, 2014
High RiskFDA
Ortho Development Corporation
Tibila Insert CK, Balanced Knee System Revision, REF563-1YYY Product Usage: UHMWPE component used in TKA and revision TKA procedures t...
Medical Devices·1 affected·Jul 11, 2014