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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:200603

CRTD COBALT HF MRI IS1 DF1, Model Number DTPB2D1; Implantable Cardioverter Defibrillators

Official recall number

Z-1781-2023

Evidence summary

Product code
NIK
Recall status
Open, Classified
Event initiated
May 10, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1781-2023

Field note

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