Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have specific model codes; contact for remedy.
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 ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. This separation could create a gap between the two pieces, potentially causing complications during medical procedures.
The Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between the two components. This separation may lead to complications during vascular procedures if the gap affects the graft's function.
Patients using the ADVANTA VXT vascular grafts with model codes 6X100, 1GDS, FH, STR-TW are affected. Medical professionals performing procedures with these grafts are at higher risk.
Check for the model code 6X100, 1GDS, FH, STR-TW on the ADVANTA VXT vascular graft. The product code is 22232 and UDI-DI is 00650862222326.
Verify the model code 6X100, 1GDS, FH, STR-TW on the vascular graft.
The recalled model is ADVANTA VXT with code 6X100, 1GDS, FH, STR-TW.
The recall record does not specify a remedy.
Check for the model code 6X100, 1GDS, FH, STR-TW and product code 22232.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1991-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1991-2024 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.
