Official recall notice

FDA DeviceClass IINotable

FDA Recall: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010

Recall date
2026-06-17
FDA class
Class II

Why it was recalled

Hazard

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

Recommended action

What to do

306 kits

Product description

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

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