Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have specific model codes and product identifiers.
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 ADVANTA VXT vascular grafts due to reports of the Slider GDS Swivel Rod separating from the Swivel Core, creating a gap between the two parts. This 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 could potentially cause complications during medical procedures if the graft is used.
Healthcare professionals using the ADVANTA VXT vascular grafts for medical procedures are likely affected. Patients receiving these grafts during surgery may be at risk if the separation occurs.
Check for product codes 22075 and UDI-DI 00650862220759 on the ADVANTA VXT vascular grafts. The specific model includes 6X80, 1GDS, FH, STR-SW.
Look for product code 22075 and UDI-DI 00650862220759 on the vascular graft.
The recall states there have been reports of separation, but the product is not currently unsafe for use. Healthcare professionals should check for the specific model codes.
Check for product code 22075 and UDI-DI 00650862220759 on the ADVANTA VXT vascular graft. The specific model includes 6X80, 1GDS, FH, STR-SW.
The recall does not specify a remedy, so contact Atrium Medical directly for guidance.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1971-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1971-2024 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.
