Device evidence

device-recall:cfres:162640

Fluid Management Convenience Kits (Angioplasty Kits) intended to be used in Fluid Management and/or Invasive Pressure Monitoring systems.

Official recall number

Z-1390-2018

Evidence summary

Product code: OEQ
Recall status: Terminated
Event initiated: January 18, 2018
Root cause: Under Investigation by firm
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1390-2018