ClearanceBrief
Recall Z-0147-2016 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

ConforMIS, Inc.

ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT and ITOTAL PS-IPOLY-IMPLANT KIT-RIGHT Catalog Number:TPS1111111

DateOct 21, 2015 (initiated Aug 31, 2015)
StatusTerminated
ReasonMay contain small amounts of ethylene glycol residue
Root causeProcess design
ActionConForMIS issued a Press on August 31, 2015 to the general public The sales force was notified through email. The sales personnel for affected accounts that had upcoming surgeries scheduled were asked to confirm that the affected surgeries were cancelled and that the devices were not used in surgery (Formal notification letters will be distributed to the affected accounts by Tuesday, September 8, 2015. The user required to confirm their understanding of the recall and to return any unused product to ConforMIS. Distribution of the letters conducted in two phases as described below: Phase 1-Surg
Quantity110 units
DistributionDistributed Nationwide and in Germany, Switzerland, and UK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K142161ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM, ITOTAL POSTERIOR STABILIZED (PS) KNEE REPLACEMENT SYSTEM
Conformis, Inc., Nov 14, 2014
K142404iTotal Posterior Stabilized (PS) Knee Replacement System
Conformis, Inc., Dec 11, 2014