ClearanceBrief
Recall Z-0585-2024 · JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Exactech, Inc.

Exactech Truliant Knee System, Catalog Numbers: a) 02-012-35-3509, b) 02-022-35-1509, c) 02-022-35-1513, d) 02-022-35-3010, e) 02-022-35-3509, f) 02-022-35-3510, g) 02-022-35-3511, h) 02-022-35-4511, i) 02-022-44-3512, j) 02-022-47-2509, k) 02-022-51-4519

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

K152170Exactech Optetrak Logic Enhanced Assembly
Exactech, Inc., Sep 3, 2015
K171045Exactech® Truliant™ Line Extensions
Exactech, Inc., Apr 28, 2017