Device evidence

device-recall:cfres:162398

LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability

Official recall number

Z-1040-2018

Evidence summary

Product code: NJL
Recall status: Terminated
Event initiated: November 29, 2017
Root cause: Packaging
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1040-2018