Medline recalls reprocessed ViewFlex Xtra ICE catheters that may contain harmful particles, risking infection or serious complications. Affected lots include specific model numbers and dates. Consumers should check their catheters and contact Medline for details.
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 ViewFlex Xtra ICE 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. This recall affects specific model numbers and production lots.
The reprocessed catheters may contain small particles of residual material from previous uses. If these particles enter the bloodstream, they can cause inflammatory responses, infections, blood clots, or serious complications like pulmonary embolism or deep vein thrombosis.
Healthcare professionals using Medline's reprocessed ViewFlex Xtra ICE catheters are most at risk. Patients receiving these catheters during procedures could also be affected if the device is used without proper safety checks.
Check for the model number D087031RH and lot numbers EP250324 through EP250724 on the catheter packaging or label. These catheters were sold with the unique identifier 20197344019554¿.
Look for the model number D087031RH and lot numbers EP250324 to EP250724 on the catheter packaging or label.
Using these reprocessed catheters may cause inflammatory responses, infections, blood clots, or serious complications like pulmonary embolism or deep vein thrombosis.
Check for the model number D087031RH and lot numbers EP250324 through EP250724 on the catheter packaging or label.
The recall record does not specify a remedy, so contact Medline directly 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-1323-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1323-2026 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.
