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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:208234

HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I

Official recall number

Z-2295-2024

Evidence summary

Product code
OJH
Recall status
Open, Classified
Event initiated
May 15, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2295-2024

Field note

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