Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected models include 6X45, 1GDS, CH, STR-SW. Product code 22092. No remedy specified in recall notice.
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 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 compromise the graft's function during medical procedures, leading to potential complications.
Patients using the recalled vascular grafts for medical procedures are most at risk. Healthcare providers who have these specific models in their inventory may also be affected.
Check for the product code 22092 on the vascular graft packaging or label. The affected models include ADVANTA VXT with specifications 6X45, 1GDS, CH, STR-SW.
Look for the product code 22092 on the vascular graft packaging or label to confirm if it's affected.
The recall notice does not specify any remedy or fix for this issue.
The affected models are ADVANTA VXT vascular grafts with specifications 6X45, 1GDS, CH, STR-SW and product code 22092.
Check for the product code 22092 on the vascular graft packaging or label. The affected models include ADVANTA VXT with specifications 6X45, 1GDS, CH, 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-1992-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1992-2024 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.
