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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:204218

24 BLOOD CULTURE KIT, REF DYNDH1632

Official recall number

Z-0313-2024

Evidence summary

Product code
GJE
Recall status
Open, Classified
Event initiated
November 01, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0313-2024

Field note

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