FDA DeviceClass IINotable
FDA Recall: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010
Description
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
Hazard
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
Remedy
306 kits
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