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taperflo™

VASCUTEK LTD · Model W40T0406CRS · UDI-DI 05037881009643

DSY Prescription
10
510(k) clearances
5,136
Adverse events (374 deaths)
86
Recalls
28
Facilities

Description

taperflo Gelatin Sealed ePTFE Vascular Prosthesis Stepped Taper with Wrap and Central Support

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.