Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have Product Code 22209 and UDI-DI 00650:086222098. Stop using if separation occurs.
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 ADVANTA VXT vascular grafts after reports of Slider GDS Swivel Rod separation. This separation could lead to complications if the graft becomes unstable during use.
The Slider GDS Swivel Rod may separate from the Swivel Core, creating a gap between the two parts. This separation could cause the graft to become unstable, potentially leading to complications during medical procedures.
Patients who have received the ADVANTA VXT vascular graft with Product Code 22209 are affected. Those with the UDI-DI 00650862222098 are at higher risk.
Check for Product Code 22209 on the ADVANTA VXT vascular graft. The UDI-DI number 00650862222098 identifies affected units.
Inspect the graft for any gap between the Slider GDS Swivel Rod and Swivel Core.
The product code is 22209.
The UDI-DI number is 00650862222098.
The recall record does not specify a remedy.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1982-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1982-2024 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.
