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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:203033

Presource Fistulogram Pack, Cat. SANOCFGHHA, Hartford Hospital, Sterile.

Official recall number

Z-0092-2024

Evidence summary

Product code
OIP
Recall status
Open, Classified
Event initiated
August 16, 2023
Root cause
Material/Component Contamination
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0092-2024

Field note

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