Atrium Medical recalls ADVANTA VXT vascular grafts due to reported slider separation risk. Affected models include 6X70, 1GDS, NH, STR-SW. No remedy stated in official notice.
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Atr: Atrium Medical is recalling specific vascular graft models (ADVANTA VXT 6X70, 1GDS, NH, STR-SW) because users reported the slider swivel rod separating from the swivel core, creating a gap. This could lead to complications during medical procedures if the graft fails to stay properly connected.
The slider swivel rod can separate from the swivel core, creating a gap between the two parts. This separation could cause the graft to malfunction during medical procedures, potentially leading to complications if the connection fails.
Medical professionals using the ADVANTA VXT vascular grafts for procedures are most at risk. Patients receiving these grafts during surgery may also be affected.
Check for the product code 22026 or UDI-DI 00650862220261 on the vascular graft. The affected models include ADVANTA VXT 6X70, 1GDS, NH, STR-SW.
Look for the product code 22026 or UDI-DI 00650862220261 on the vascular graft.
The official recall notice does not state any remedy.
The official recall notice does not specify any action steps.
Check for the product code 22026 or UDI-DI 00650862220261 on the vascular graft. Affected models include ADVANTA VXT 6X70, 1GDS, NH, STR-SW.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1959-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1959-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
