Atrium Medical recalls ADVANTA VXT vascular grafts (model 4-7X45, 2GDS) due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between components.
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 specific ADVANTA VXT vascular graft models because users have reported the Slider GDS Swivel Rod separating from the Swivel Core, creating a gap. This could potentially lead to complications during medical procedures if the graft fails to stay properly connected.
The Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between the two components. This separation might cause the graft to malfunction during medical procedures, potentially leading to complications if the connection fails.
Patients who have received the specific ADVANTA VXT vascular graft models (4-7X45, 2GDS) from Atrium Medical are most at risk. Healthcare providers using these grafts in procedures may also be affected.
Check for the product code 22297 or UDI-DI 00650862222975 on the vascular graft. The affected models are labeled as ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS.
Look for the product code 22297 or UDI-DI 00650862222975 on the vascular graft.
The recall is due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between the two components.
The affected models are ADVANTA VXT vascular grafts with the product code 22297 and UDI-DI 00650862222975, specifically labeled as 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS.
The recall record does not mention any remedy or fix for this issue.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1997-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1997-2024 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.
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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.
