Medline Industries recalled 228 lots of ReNewal Reprocessed Webster CS Catheters on December 22, 2025. These catheters may contain small particles that pose serious health risks, including systemic infection. Patients must stop using them immediately and follow the recall instructions.
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
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
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The recall affects several models of Webster CS Catheters, including BD710DF282CRH, BD710DF282RRH, BD710FJ282RRH, and BD710FJ282CRH. These catheters were distributed nationwide in the United States.
The affected catheters may contain small particles of residual material, leading to serious health risks. Risks include inflammatory responses, systemic infections, or thrombus reactions that could result in cerebral or pulmonary embolisms.
To date, there are no reported injuries or fatalities directly linked to the use of the affected catheters. However, the potential for serious complications exists.
Patients and healthcare providers should immediately stop using the affected devices. Contact Medline Industries for further instructions regarding the recall.
For more information, call Medline Industries at 1-800-633-5463 or visit their website. The recall is also detailed on the FDA's website.
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