Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have specific model codes and UDI-DI numbers. Contact for remedy details.
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 reported separation of the Slider GDS Swivel Rod from the Swivel Core. This separation creates a notable gap between the two parts, which could lead to complications during medical procedures.
The Slider GDS 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.
Patients using the recalled vascular grafts for medical procedures are most at risk. Healthcare providers who have the affected models in their inventory should also check their equipment.
Check for the product code 22070 and UDI-DI number 00650862220704 on the vascular graft. The affected models include ADVANTA VXT, 6X70, 1GDS, FH, STR-SW.
Look for the product code 22070 and UDI-DI number 00650862220704 on the vascular graft.
The recalled models are ADVANTA VXT, 6X70, 1GDS, FH, STR-SW with product code 22070 and UDI-DI 00650862220704.
The recall record does not specify a remedy.
Check for the product code 22070 and UDI-DI number 00650862220704 on the graft.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1968-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1968-2024 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.
