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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:210028

Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006, MON-000006-RFB.

Official recall number

Z-0051-2025

Evidence summary

Product code
EOQ
Recall status
Open, Classified
Event initiated
August 02, 2024
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0051-2025

Field note

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