Quick Facts at a Glance
- Recall Date
- November 26, 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
- IV Administration Set
- Model numbers
- UDI/DI 10884389725092 (EA) 40884389725093 (CS), Lot number 25IBC144
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 26, 2025
Reported by FDA DEVICE
January 21, 2026
RecallRadar source check
April 13, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
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 IV Administration Sets are used in healthcare settings to deliver medications and fluids intravenously. These products are essential for patient care in various medical procedures.
Why This Is Dangerous
The malfunction of the check valve components can disrupt the flow of medication, which may lead to serious complications in patient treatment.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients relying on these IV administration sets may face significant health risks. Immediate action is required to ensure safety.
Practical Guidance
How to identify if yours is affected
- Verify the model numbers: UDI/DI 10884389725092 and 40884389725093.
- Check the lot number: 25IBC144.
- Review the notification letter received from Medline.
Where to find product info
Model numbers and lot numbers can be found on the packaging or product label of the IV sets.
What timeline to expect
Expect a refund or replacement processing time of about 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with Medline.
- Contact the FDA or CPSC for further assistance if needed.
How to prevent similar issues
- Always check for recalls before using medical devices.
- Look for safety certifications on medical products.
- Ensure proper training for healthcare professionals using IV administration sets.
Documentation advice
Keep records of your correspondence regarding the recall, including dates and descriptions of communication.
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Product Details
The recall involves Medline kits containing B. Braun IV Administration Sets and Pump Administration Sets, specifically labeled as NEURO ANGIO PACK, Medline kit SKU DYNJ38935. The affected models include UDI/DI 10884389725092 (EA) and 40884389725093 (CS), with lot number 25IBC144.
Key Facts
- Recall date: November 26, 2025
- Affected models include UDI/DI 10884389725092 and 40884389725093
- Lot number 25IBC144
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Safety Guide
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