Atrium Medical recalls ADVANTA VXT vascular grafts due to reported slider separation risks. Affected models include 6X50, 1GDS, NH, STR-SW. No remedy specified in official notice.
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 graft models because users have reported the slider swivel rod separating from the swivel core, creating a gap between parts. This could lead to complications during medical procedures if the graft fails to stay properly connected.
The hazard involves the slider swivel rod potentially separating from the swivel core, creating a gap between the two components. This separation could compromise the graft's integrity during medical procedures, leading to potential complications if the connection fails.
Patients using the ADVANTA VXT vascular graft models (6X50, 1GDS, NH, STR-SW) for medical procedures are most at risk. Healthcare providers who use these grafts in surgeries may also be affected.
Check for the product code 22017 and UDI-DI 00650862220179 on the vascular graft. Affected models include ADVANTA VXT with specifications 6X50, 1GDS, NH, STR-SW.
Look for the product code 22017 and UDI-DI 00650862220179 on the vascular graft to confirm if it is affected.
The official recall notice does not specify any remedy.
Affected models include ADVANTA VXT vascular grafts with specifications 6X50, 1GDS, NH, STR-SW.
Check for the product code 22017 and UDI-DI 00650862220179 on the graft. The specific model numbers listed in the recall are 6X50, 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-1955-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1955-2024 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.
