FDA DeviceClass IINotable

FDA Recall: PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)108019021

Date: 2026-04-29
Brand: ARROW INTERNATIONAL, LLC
Category: Medical Device
FDA Class: Class II

Description

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Remedy

115

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