Atrium Medical recalls ADVANTA VXT vascular grafts due to reported slider separation risk. Affected models include 8X70, 1GDS, NH, STR-SW. 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.
Atrium Medical is recalling specific ADVANTA VXT vascular graft models because users have reported the slider swivel rod separating from the swivel core, creating a gap between the parts. This could lead to complications during medical procedures if the graft fails to stay properly connected.
The slider 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 if the connection fails.
Medical professionals using the ADVANTA VXT vascular grafts with model numbers 8X7: 1GDS, NH, STR-SW are most at risk. Patients receiving these grafts during surgery may also be affected.
Check for the model numbers 8X70, 1GDS, NH, STR-SW on the ADVANTA VXT vascular graft. The product code is 22028 and UDI-DI is 00650862220285.
Look for model numbers 8X70, 1GDS, NH, STR-SW on the vascular graft.
The recall is due to reported separation of the slider swivel rod from the swivel core, which could cause the graft to malfunction during medical procedures.
Check for model numbers 8X70, 1GDS, NH, STR-SW on the ADVANTA VXT vascular graft. The product code is 22028 and UDI-DI is 00650862220285.
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-1961-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1961-2024 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.
