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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:198347

CardioMEMS HF System Patient Electronics System (PES), Model number CM1010, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data used for the monitoring and management of heart failure (HF) patients. The system measures changes in PA pressure which physicians use to initiate or modify heart failure treatment.

Official recall number

Z-1219-2023

Evidence summary

Product code
MOM
Recall status
Open, Classified
Event initiated
February 07, 2023
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1219-2023