Atrium Medical recalls ADVANTA VXT vascular grafts 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 ADVANTA VXT vascular grafts after complaints about the Slider GDS Swivel Rod separating from the Sw: Swivel Core, creating a gap. This could 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 parts. This separation might cause the graft to malfunction during medical procedures, potentially leading to complications if the connection fails.
Patients who have received the ADVANTA VXT vascular grafts with the specific model numbers mentioned in the recall are affected. Medical professionals using these grafts during procedures are at risk if the separation occurs.
Check for the product code 22012 and UDI-DI 00650862220124 on the ADVANTA VXT vascular grafts. The specific model numbers include 6X40, 1GDS, NH, STR-SW.
Look for the product code 22012 and UDI-DI 00650862220124 on the vascular graft.
The recall is due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, which could cause a gap between components. However, the hazard is described as a reported issue, not a confirmed risk of serious injury.
The recall does not specify a remedy, so there are no immediate actions required. Check the product details to confirm if you have the recalled model.
Check for the product code 22012 and UDI-DI 00650862220124 on the ADVANTA VXT vascular graft. The specific model numbers include 6X40, 1GDS, NH, STR-SW.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1952-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1952-2024 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.
