Atrium Medical recalls ADVANTA VXT vascular grafts (model 4-7X80, 1GDS, FH, TPR-TW) 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 hazard involves the Slider GDS Swivel Rod potentially separating from the Swivel Core, creating a gap between the two parts. This separation could compromise the graft's function during medical procedures, potentially leading to complications if the connection fails.
Patients using the recalled ADVANTA VXT vascular grafts (model 4-7X80, 1GDS, FH, TPR-TW) are most at risk. Healthcare providers who have implanted these grafts may also need to check their devices.
Check for the product code 22266 or UDI-DI 00650862222661 on the device. The recalled models are ADVANTA VXT vascular grafts with specific dimensions (4-7X80, 1GDS, FH, TPR-TW).
Look for the product code 22266 or UDI-DI 00650862222661 on the device label.
The recall is due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between components.
Check the device for the product code 22266 or UDI-DI 00650862222661. If you have the recalled model, contact Atrium Medical for further instructions.
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-2000-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-2000-2024 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.
