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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:113443

AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Regular. AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional devices within the vasculature.

Official recall number

Z-0134-2013

Evidence summary

Product code
DQX
Recall status
Terminated
Event initiated
July 27, 2012
Root cause
Equipment maintenance
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0134-2013