Angiodynamics recalls XCELA ports due to potential delay in implantation procedures. Learn what to do if you own this device.
Snap lock connectors provided within implantable port kits may not meet dimensional specifications, and the catheter cannot be inserted into the snap lock connector prior to connection to the port chamber, resulting in a delay to the implantation procedure.
Angiodynamics recalls XCELA ports that may cause delays during implantation procedures. This recall affects patients needing long-term central venous access.
The snap lock connectors in the port kits may not meet precise size requirements. This can cause the catheter to not connect properly with the port chamber, delaying the implantation procedure.
Patients with central venous access needs, such as those receiving chemotherapy or blood products. Those who have recently had the port implanted are most at risk.
Check for the XCELA port model with the serial number H965440400 and catalog number 44-040. This device is used for long-term central venous access for fluids and blood products.
Look for the XCELA port model with serial number H965440400 and catalog number 44-040.
The snap lock connectors may not meet dimensional specifications, which can delay the implantation procedure.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
The recall indicates a potential delay in implantation procedures, but no immediate safety risk to users.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0505-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-0505-2020 from Angiodynamics. 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.
