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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:165916

DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries

Official recall number

Z-2971-2018

Evidence summary

Product code
HBL
Recall status
Terminated
Event initiated
July 05, 2018
Root cause
Component change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2971-2018

Field note

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