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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209236

KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.

Official recall number

Z-0049-2025

Evidence summary

Product code
IQZ
Recall status
Open, Classified
Event initiated
August 22, 2024
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0049-2025

Field note

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