FDA DeviceClass IINotable
FDA Recall: React Health PHOENIX 5L Oxygen Concentrator
Description
Devices which did not meet internal quality specifications were inadvertently distributed.
Hazard
Devices which did not meet internal quality specifications were inadvertently distributed.
Remedy
2 units
Related Recalls
2026-06-17 · FDA_DEVICE
FDA Recall: Allia Moveo angiographic X-ray system
GE Medical Systems, LLC
2026-06-17 · FDA_DEVICE
FDA Recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
INSPIREMD Inc
2026-06-17 · FDA_DEVICE
FDA Recall: Plum Solo Precision IV Pump, 40001-0401
ICU Medical, Inc.
2026-06-17 · FDA_DEVICE
FDA Recall: Allia IGS 3 Pulse angiographic X-ray system
GE Medical Systems, LLC