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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:196289

CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST

Official recall number

Z-0212-2023

Evidence summary

Product code
KCT
Recall status
Open, Classified
Event initiated
September 26, 2022
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0212-2023