Medline recalls specific lots of reprocessed cardiac catheters that may contain small particles. Using these could cause infections or blood clots. Affected items have unique identifiers and lot numbers listed in the recall.
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Medline is recalling specific lots of reprocessed Webster CS Catheter 10 Electrodes that may contain small particles. If these particles enter the bloodstream during use, they could cause infections, blood clots, or serious complications like pulmonary embolism.
The catheters may have small particles from reprocessing that can enter the bloodstream. If these particles dislodge and interact with blood or the heart, they might cause infections, blood clots, or serious complications like pulmonary embolism.
Healthcare professionals using these catheters for cardiac procedures are most at risk. Patients undergoing electrophysiological mapping with the recalled devices could face complications.
Check for lot numbers EP241216 through EP250210 on the catheter packaging. The item numbers include BD710DF282CRH, BD710DF282RRH, BD710FJ282CRH, or BD710FJ282RRH with specific serial numbers.
Verify the item numbers on the catheter packaging to see if they match the listed BD710DF282CRH, BD710DF282RRH, BD710FJ282CRH, or BD710FJ282RRH with the provided serial numbers.
Reach out to Medline directly for further assistance or to confirm if your specific catheter is affected.
The catheters may contain small particles from reprocessing that could enter the bloodstream, leading to infections, blood clots, or serious complications like pulmonary embolism.
Check for lot numbers EP241216 through EP250210 and item numbers BD710DF282CRH, BD710DF282RRH, BD710FJ282CRH, or BD710FJ282RRH with the listed serial numbers.
Contact Medline directly to confirm if your catheters are affected and for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2611-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2611-2025 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.
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.