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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Medline Industries, LP
- Product type
- Catheters
- 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
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 22, 2025
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
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
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
- Check the model number against the recall list provided by Medline.
- Verify the lot number of your catheter to confirm if it is affected.
- 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.
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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
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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