Medline recalls reprocessed Webster CS catheters with potential residual particles that could cause infection or serious complications. Affected lots include specific model numbers and production dates. Consumers should stop using these catheters if they have the listed models.
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 Webster CS catheters that may contain small particles of residual material. Using these catheters could lead to infections, inflammation, or serious blood clots that might cause life-threatening complications.
The catheters may contain small particles of residual material from reprocessing. If used, these particles can cause an inflammatory response, infection, or blood clots that might lead to serious complications like pulmonary embolism or deep vein thrombosis.
Healthcare professionals and patients using the recalled catheters are at risk. Those with the specific model numbers and production dates listed in the recall are most affected.
Check for the model numbers BD710DF282CRH, BD710DF282RRH, BD710FJ282RRH, or BD710FJ282CRH with UDI-DI numbers 10197344044023, 10197344044030, or 10197344044054. The recall covers catheters produced between EP250429 and EP250808.
Immediately stop using the recalled catheters if you have the specific model numbers and UDI-DI numbers listed in the recall.
These catheters may contain small particles of residual material from reprocessing, which could cause inflammation, infection, or blood clots leading to serious complications like pulmonary embolism or deep vein thrombosis.
Affected models include BD710DF282CRH, BD710DF282RRH, BD710FJ282RRH, and BD710FJ282CRH with specific UDI-DI numbers and production dates.
Check the model number and UDI-DI number on the catheter packaging. The recall covers specific production dates (EP250429 to EP250808) and model numbers listed in the notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1319-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1319-2026 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.
