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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:194238

Legacy Base for Dual Bed Configurations

Official recall number

Z-1500-2022

Evidence summary

Product code
LLI
Recall status
Open, Classified
Event initiated
March 24, 2017
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1500-2022