ClearanceBrief
Recall Z-2636-2016 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Medtronic Sofamor Danek USA Inc

TIBIAL TRAY , SIZE 3, REF 90-SRK-200300, QTY: 1, STERILE R, total knee replacement

DateJul 18, 2016
StatusTerminated
ReasonThe alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
Root causeEmployee error
ActionOn 07/18/2016, the firm initiated the correction by verbally notifying (by visit and telephone) three of four (3 of 4) implanting surgeons; the fourth implanting surgeon was verbally notified on 07/25/2016. The firm followed with a letter to all four (4) surgeons on 07/28/2016. Medtronic recommended that the condition of the patients receiving the subject part be assessed for any indications of premature failure during normal post-operative follow-up visits.
Quantity3 units
DistributionAR, MN,MA
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K150496Total Knee Arthroplasty System
Responsive Orthopedics, LLC, Jun 12, 2015