ClearanceBrief
Recall Z-1267-2023 ยท OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive

DePuy Orthopaedics, Inc.

Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507

DateMar 17, 2023 (initiated Feb 15, 2023)
StatusOpen, Classified
ReasonThe subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material properties.
Root causeLabeling Change Control
ActionAn URGENT MEDICAL DEVICE RECALL (REMOVAL) notification letter dated 2/14/23 was delivered to customers. Please Take the Following Steps: 1. Examine your inventory immediately to determine if you have the subject products and quarantine the subject products. DO NOT USE THE SUBJECT PRODUCTS. 2. Contact your DePuy Synthes Sales Consultant to coordinate the return/credits of the subject products. 3. Review, complete, sign, and return the attached Business Response Form (See page 3 of this communication) to OneMD-Field-Actions@its.jnj.com within three (3) business days of receipt of this notificat
Quantity12 units
DistributionWorldwide distribution - US Nationwide and the countries of Canada, Poland, Germany, India, Australia, & New Zealand
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K111433DEPUY STTUNE (TM) PS KNEE SYSTEM
DePuy Orthopaedics, Inc., Aug 30, 2011