HIGH

Medline Catheters Recalled Over Infection Risk

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.

Quick Facts at a Glance

Recall Date
December 22, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

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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About This Product

Medline ReNewal Reprocessed Webster CS Catheters are used in various medical procedures requiring catheterization. They are designed to be reprocessed for multiple uses, appealing to healthcare facilities for cost-saving measures.

Why This Is Dangerous

The recall is due to potential residual particles in the catheters, which may lead to serious health complications such as infections or embolisms when used in patients. This poses a significant risk to patient safety.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall could lead to significant safety concerns for patients relying on these catheters, potentially resulting in health complications if not addressed promptly.

Practical Guidance

How to identify if yours is affected

  1. Check the model number against the recall list provided by Medline.
  2. Verify the lot number of your catheter to confirm if it is affected.
  3. Contact your healthcare provider for further instructions.

Where to find product info

Model and lot numbers are typically found on the packaging of the catheter or the device itself.

What timeline to expect

Expect refund processing to take approximately 4-6 weeks once the return is initiated.

If the manufacturer is unresponsive

  • Document all correspondence with Medline.
  • Follow up with a phone call or email to inquire about your refund status.
  • Consider filing a complaint with the FDA if there is no response.

How to prevent similar issues

  • Always use single-use catheters if possible to avoid reprocessing risks.
  • Ensure all medical devices are obtained from reputable suppliers with safety certifications.
  • Stay informed about product recalls through FDA notifications.

Documentation advice

Keep a record of your purchase, the recall notification, and any communication with Medline for your records.

Product Details

The recall affects several models of Webster CS Catheters, including BD710DF282CRH, BD710DF282RRH, BD710FJ282RRH, and BD710FJ282CRH. These catheters were distributed nationwide in the United States.

Key Facts

  • Recall affects 228 lots of catheters
  • Potential for serious infection risks
  • Consumers must stop using devices immediately
  • Contact Medline for return instructions

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
BD710DF282CRH UDI-DI 10197344044023 Lots EP250429 EP250808
BD710DF282RRH UDI-DI 10197344044030 Lots EP250429 EP250808
BD710FJ282RRH UDI-DI 10197344044054 Lots EP250429 EP250808
BD710FJ282CRH UDI-DI (case) 40197344044048 (ea) 10197344044047 Lots EP250429 EP250808
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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