ClearanceBrief
Recall Z-0800-2011 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Encore Medical, Lp

Turon Shoulder System Instrumentation, Turon Trial Pegged Glenoid, DJO Surgical

DateDec 22, 2010 (initiated Nov 5, 2010)
StatusTerminated
ReasonComplaints of fracturing were reported for affected trial products.
Root causeDevice Design
ActionEncore Medical notified consignees by letter on 11/5/2010.
Quantity85 units
DistributionTX, FL, SC, GA
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K080402ENCORE SHOULDER PRIMARY HUMERAL STEM, MODEL 500-00, ENCORE SHOULDER HUMERAL HEAD, MODEL 520-38
Encore Medical L.P., Mar 28, 2008