Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199178

EMPOWR Porous Knee Patella Over Drill, REF: 802-05-104; EMPOWR Knee Patella Drill, REF: 802-05-108

Official recall number

Z-1384-2023

Evidence summary

Product code
MBH
Recall status
Open, Classified
Event initiated
February 28, 2023
Root cause
Process change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1384-2023