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HomeMAQUET CARDIOVASCULAR LLC › Exxcel Soft ePTFE Vascular Graft

Exxcel Soft ePTFE Vascular Graft

MAQUET CARDIOVASCULAR LLC · Model M002004910460 · UDI-DI 00384409002002

DSY Prescription
1
510(k) clearances
5,136
Adverse events (374 deaths)
86
Recalls
28
Facilities

Description

EXXCEL SOFT THIN WALL STR 6/40

Recalls

DateFirmReason
2025-12-18Vascutek, Ltd.Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry should have been cal
2025-08-26W L Gore & Associates, Inc.Reports of vascular graft delamination, which may lead to reduced access flow; cannulation difficulties; bleeding or bruising; and harms related to reintervention procedures, so In
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
2024-05-03Atrium Medical CorporationComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.