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Prosthesis, Vascular Graft, Of Less Then 6mm Diameter

FDA product code DYF · Class 2 · Cardiovascular

487
Registered devices
193
Adverse events
17
Recalls
21
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
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.
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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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.