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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:185073

ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston Scientific coronary venous lead is positioned.

Official recall number

Z-0870-2021

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
December 15, 2020
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0870-2021

Field note

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