Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have specific product codes; contact for remedy.
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Atr:ium Medical is recalling certain ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. This separation could create a gap between the two parts, potentially causing complications during medical procedures.
The Slider GDS Swivel Rod may separate from the Swivel Core, creating a gap between the two parts. This separation could lead to complications during medical procedures if the graft is used.
Patients using the ADVANTA VXT vascular grafts with the specific product codes (22063) are affected. Medical professionals who have implanted these grafts are most at risk.
Check for the product code 22063 on the vascular graft. The UDI-DI number 00650862220636 is also associated with this model.
Look for the product code 22063 on the vascular graft to confirm if it is affected.
The recall reports separation of the Slider GDS Swivel Rod from the Swivel Core, but no specific injuries or deaths have been reported. The hazard is described as a potential complication during medical procedures.
Check for the product code 22063 or the UDI-DI number 00650862220636 on the vascular graft.
The recall does not specify a remedy, so contact Atrium Medical for further instructions.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1966-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1966-2024 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.
