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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:208259

Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101

Official recall number

Z-2221-2024

Evidence summary

Product code
GCJ
Recall status
Completed
Event initiated
June 03, 2024
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2221-2024

Field note

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