Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between components.
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Atrium Medical is recalling specific ADVANTA VXT vascular grafts because users have reported the Slider GDS Swivel Rod separating from the Sw: Swivel Core, creating a gap between the two parts. This separation could lead to complications during medical procedures.
The Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between the two components. This separation may cause the graft to malfunction during medical procedures, potentially leading to complications.
Patients using the ADVANTA VXT vascular grafts with the specific model numbers (8X50, 1GDS, NH, STR-SW) are affected. Medical professionals performing procedures with these grafts are at higher risk.
Check for the product code 22019 or UDI-DI 00650862220193 on the vascular graft. The affected models include ADVANTA VXT, 8X50, 1GDS, NH, STR-SW.
Look for the product code 22019 or UDI-DI 00650862220193 on the vascular graft.
The recall is due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between the two components.
Check for the product code 22019 or UDI-DI 00650862220193 on the vascular graft. If you have the affected model, contact Atrium Medical for further instructions.
The recall record does not mention a specific fix or remedy for this issue.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1957-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1957-2024 from Atrium Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
