Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected models include 7X70, 1GDS, FH, STR-SW. Product code 22071. 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 affecting the graft's function during medical procedures.
The Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between the two components. This separation may compromise the graft's structural integrity during medical procedures, potentially leading to functional issues or complications.
Patients using the ADVANTA VXT vascular graft models with product code 22071 are affected. Medical professionals who have implanted these grafts are most at risk of complications if the separation occurs.
Check for the product code 22071 on the ADVANTA VXT vascular graft. The affected models include 7X70, 1GDS, FH, STR-SW. These grafts were sold with UDI-DI: 00650862220711.
Look for product code 22071 on the ADVANTA VXT vascular graft to confirm if it is affected.
The recall notice does not specify any remedy for this issue.
The affected models are ADVANTA VXT vascular grafts with product code 22071, including 7X70, 1GDS, FH, STR-SW.
Check for product code 22071 on the graft. Affected models include 7X70, 1GDS, FH, STR-SW with UDI-DI: 00650862220711.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1969-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1969-2024 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.
