Medline recalls reprocessed Siemens ACUSON AcuNav ultrasound catheters used on GE systems due to potential small particles causing infection or serious complications. Affected units have specific model numbers and lot codes.
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Medline is recalling reprocessed Siemens ACUSON AcuNav ultrasound catheters that may contain small particles of residual material. Using these catheters could lead to infections, blood clots, or serious health issues like pulmonary embolism.
The reprocessed catheters may have small particles of residual material that, if used, can cause inflammatory responses, infections, or blood clots. This could lead to serious conditions like pulmonary embolism or deep vein thrombosis.
Healthcare professionals using these catheters for medical imaging are most at risk. Patients receiving procedures with the recalled units could face complications.
Check for model numbers 10135910RH, 10043342RH, 10135936RH, or 08255790RH on the catheter. Also look for lot codes EP250324 through EP250905.
Immediately stop using any catheters with model numbers 10135910RH, 10043342RH, 10135936RH, or 08255790RH and lot codes EP250324 through EP250905.
Using these reprocessed catheters may cause inflammatory responses, infections, or blood clots, which could lead to serious complications like pulmonary embolism or deep vein thrombosis.
Affected model numbers include 10135910RH, 10043342RH, 10135936RH, and 08255790RH.
The recall includes lot codes EP250324, EP250429, EP250521, EP250609, EP250630, EP250710, and EP250905.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1325-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1325-2026 from Medline. 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.
