Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected models include 8X70, 1GDS, FH, STR-SW. Product code 22072; UDI-DI 00650:86220728.
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 grafts 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 Slider GDS Swivel Rod may separate from the Swivel Core, creating a gap between the two components. This separation could lead to complications during medical procedures if the gap affects the graft's function.
Patients using the recalled vascular grafts for medical procedures. Healthcare providers who have the affected models are most at risk.
Check for the product code 22072 and UDI-DI 00650862220728 on the vascular graft packaging or label. The affected models include ADVANTA VXT, 8X70, 1GDS, FH, STR-SW.
Look for the product code 22072 and UDI-DI 00650862220728 on the vascular graft packaging or label.
The recall is due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, which creates a gap between the two parts.
The affected models are ADVANTA VXT, 8X70, 1GDS, FH, STR-SW with product code 22072 and UDI-DI 00650862220728.
The recall record does not specify a remedy, so check with Atrium Medical for further instructions.
We’ve drafted a message you can send Atrium Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1970-2024 — Atrium Medical Atrium Medical Hello, I own a Atrium Medical that is covered by recall Z-1970-2024 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.
