Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected models include 8X80, 1GDS, FH, STR-TW. Product code 22227; UDI-DI 00650:0862222272. No remedy specified.
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 gap between the two parts, potentially causing complications during medical procedures.
The hazard involves the Slider GDS Swivel Rod separating from the Swivel Core, creating a noticeable gap between the two components. This separation could compromise the graft's function during medical procedures, potentially leading to complications.
Patients using the ADVANTA VXT vascular graft models listed in the recall are affected. Medical professionals who have implanted these grafts are most at risk.
Check for the product code 22227 and UDI-DI 00650862222272 on the device. Affected models include ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS Vascular grafts.
Look for the product code 22227 and UDI-DI 00650862222272 on the device.
The recall record does not specify any remedy.
Affected models include ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS Vascular grafts with product code 22227 and UDI-DI 00650862222272.
Check for the product code 22227 and UDI-DI 00650862222272 on the device. Affected models include ADVANTA VXT, 8X80, 1GDS, FH, STR-TW.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1990-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1990-2024 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.
