ClearanceBrief
Recall Z-2156-2024 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Exactech, Inc.

OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM; b) 200-03-29, 29MM; c) 200-03-32, 32MM; d) 200-03-35, 35MM; e) 200-03-38, 38MM; f) 200-03-41, 41MM

DateJun 18, 2024 (initiated Apr 18, 2024)
StatusOpen, Classified
ReasonExactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Root causeUnder Investigation by firm
ActionExactech issued an URGENT VOLUNTARY MEDICAL DEVICE RECALL to its sales representatives on 04/12/2024. The notice explained the issue with the device, clinical impact (risk), and requested the following: Actions to be Taken " Review this notification thoroughly. " Immediately discontinue use and quarantine any affected product. " Send all affected product back to Exactech as outlined in the attached Recall Confirmation Form . The firm notified the surgeons, hospitals, and healthcare professionals on 04/18/2024. That notice also explained the issue, clinical impact (risk) and requested th
DistributionWorldwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K160484Optetrak Advanced Patella
Exactech, Inc., Mar 18, 2016
K932690EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY
Exactech, Inc., Feb 9, 1995
K933610EXACTECH CEMENTED TOTAL KNEE SYSTEM, TIBIAL COMPONENTS
Exactech, Inc., Jan 17, 1995