Atrium Medical recalls ADVANTA VXT vascular grafts (4-7X7:1GDS, NH, TPR-SW) due to reported separation of Slider GDS Swivel Rod from 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 grafts because users have reported the Slider GDS Swivel Rod separating from the Swivel Core, creating a gap. This separation 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 if the connection fails to stay secure.
Patients using the recalled ADVANTA VXT vascular grafts (model 4-7X70, 1GDS, NH, TPR-SW) are most at risk. Healthcare providers who have implanted these grafts may also be affected.
Check for the product code 22117 or UDI-DI 00650862221176 on the graft. The specific model is 4-7X70, 1GDS, NH, TPR-SW.
Look for the product code 22117 or UDI-DI 00650862221176 on the graft.
The recall is based on reported separations of the Slider GDS Swivel Rod from the Swivel Core, but no injuries have been reported. The risk level is low.
Check for the product code 22117 or UDI-DI 00650862221176 on the graft. The specific model is 4-7X70, 1GDS, NH, TPR-SW.
The recall does not specify a remedy, so contact Atrium Medical for further guidance.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1996-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1996-2024 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.
