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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:167204

VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker)

Official recall number

Z-3258-2018

Evidence summary

Product code
LWS
Recall status
Terminated
Event initiated
September 10, 2018
Root cause
Component design/selection
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-3258-2018

Field note

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