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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:167467

Synchro2, 0.014in. x 300cm, SOFT PRE-SHAPED Guidewire with Hydrophilic Coating, UPN Product No. M00326320, REF 2632, STERILE:EO - Product Usage: product is intended for general intravascular use, including neurovascular and peripheral vasculatures.

Official recall number

Z-0228-2020

Evidence summary

Product code
DQX
Recall status
Terminated
Event initiated
June 08, 2018
Root cause
Employee error
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0228-2020

Field note

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