Atrium Medical recalls FLIXENE vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have a gap between components, posing a potential risk of disconnection during use.
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 FLIXENE vascular grafts (product code 25059) due to complaints about the Slider GDS Swivel Rod separating from the Swivel Core, creating a gap between the two parts. This separation could lead to the graft becoming disconnected during use, which may cause complications for patients.
The Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between the two components. This separation may cause the vascular graft to become disconnected during use, potentially leading to complications for patients.
Patients who have received FLIXENE vascular grafts (product code 25059) from Atrium Medical are likely affected. Those with the specific product model are at risk if the Slider GDS Swivel Rod separates from the Swivel Core.
Check for the product code 25059 on the FLIXENE vascular graft. The specific model is described as '7X50, 1GDS, GW. Single-Ended Slider GDS.'
Look for product code 25059 on the FLIXENE vascular graft.
Atrium Medical recalls FLIXENE vascular grafts due to complaints about the Slider GDS Swivel Rod separating from the Swivel Core, creating a gap between the two parts.
Check for product code 25059 on the FLIXENE vascular graft. The specific model is described as '7X50, 1GDS, GW. Single-Ended Slider GDS.'
The recall record does not specify a remedy, so no action is required beyond checking if you have the product code 25059.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2003-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-2003-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
