Official recall notice

FDA DeviceClass IINotable

FDA Recall: Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

Recall date
2026-04-22
FDA class
Class II

Why it was recalled

Hazard

Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

Recommended action

What to do

713,702 units

Product description

Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

Verify with the official notice →
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