ClearanceBrief
Recall Z-0583-2024 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Exactech, Inc.

Exactech Optetrak Logic Knee System, Catalog Numbers: a) 02-012-47-3011, b) 02-012-47-5009, c) 02-012-47-5011, d) 02-012-65-3013

DateJan 18, 2024 (initiated Nov 21, 2023)
StatusOpen, Classified
ReasonExactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Root causePackaging change control
ActionExactech issued an URGENT MEDICAL DEVICE RECALL notice to its direct consignees on 11/21/2023 via email. The notice explained the issue, clinical impact, and requested the removal and return of all affected products. 11/22/2023, the firm initiated the recall OUS also by email.
DistributionUS NY, TX, IN, IL, MN, KY, VA, MD, TN, GA, NH, ME, SC, NV, FL, AR and Australia, Brazil, Chile, France, Germany, Guatemala, Italy, Japan, Korea, Slovenia, Spain, UK
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K111400OPTETRAK LOGIC CR TIBIAL INSERT, OPTETRAK LOGIC CR FEMORAL COMPONENT
Exactech, Inc., Jul 28, 2011
K150890Exactech Optetrak Logic CC
Exactech, Inc., May 29, 2015