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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:184628

Cardiac Pack - LF, Model DYNJ31903I - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Official recall number

Z-0783-2021

Evidence summary

Product code
OEZ
Recall status
Terminated
Event initiated
November 13, 2020
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0783-2021

Field note

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