Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation risk. Affected models include 4-6X45, 1GDS, CH, TPR-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 due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. This separation could create a notable gap between the two parts, potentially causing complications during medical procedures.
The hazard involves the Slider GDS Swivel Rod potentially separating from the Swivel Core, creating a gap between the two components. This separation could lead to mechanical failure during medical procedures, affecting the graft's function and patient safety.
Patients using the recalled ADVANTA VXT vascular grafts for medical procedures are affected. Healthcare providers who have installed these grafts are most at risk of complications if the separation occurs.
Check for the product code 22124 and UDI-DI 00650862221244 on the vascular graft. The affected models include ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW.
Verify the product code 22124 and UDI-DI 00650862221244 on the vascular graft.
The official recall notice does not specify any remedy.
The affected models are ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW with product code 22124 and UDI-DI 00650862221244.
Check for the product code 22124 and UDI-DI 00650862221244 on the vascular graft.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1998-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1998-2024 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.
