Atrium Medical recalls FLIXENE vascular grafts with reported slider swivel rod separation. Affected units have a gap between slider and core. Contact for remedy details.
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 after reports of the slider swivel rod separating from the core, creating a gap between the two parts. This could lead to complications during medical procedures.
The slider swivel rod can separate from the swivel core, creating a gap between the two parts. This separation could cause the graft to malfunction during medical procedures, potentially leading to complications.
Patients using this vascular graft during surgery or medical procedures are most at risk. The recall affects specific model numbers sold under the FLIXENE brand.
Check for the product code 25052 on the FLIXENE vascular graft packaging. The UDI-DI number 00650862250527 is also associated with this specific model.
Look for product code 25052 or UDI-DI number 00650862250527 on the vascular graft packaging.
The recall is due to reported separation of the slider swivel rod from the swivel core, creating a gap between the two parts.
The official recall notice does not specify a remedy or action steps for affected products.
Check for product code 25052 or UDI-DI number 00650862250527 on the vascular graft packaging.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2009-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-2009-2024 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.