FDA DeviceClass IINotable
FDA Recall: PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)108019021
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
Related Recalls
2026-05-20 · FDA_DEVICE
FDA Recall: Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I
ARROW INTERNATIONAL, LLC
2026-05-20 · FDA_DEVICE
FDA Recall: NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-
ARROW INTERNATIONAL, LLC
2026-05-20 · FDA_DEVICE
FDA Recall: Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, A
ARROW INTERNATIONAL, LLC
2026-05-20 · FDA_DEVICE
FDA Recall: Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, C
ARROW INTERNATIONAL, LLC