Quick Facts at a Glance
- Recall Date
- December 5, 2025
- Hazard Level
- HIGH
- Brand
- LimFlow
- Category
- Health & Personal Care
- Sold At
- Unknown
- 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
- LimFlow
- Product type
- Medical Device
- Model numbers
- Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 5, 2025
Reported by FDA DEVICE
February 4, 2026
RecallRadar source check
February 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Incorrect expiration date
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact LimFlow, Inc. or your healthcare provider for instructions. Notification method: Letter
About This Product
The LimFlow Vector is a medical device designed for specific healthcare applications. Patients and healthcare providers rely on its proper functionality for treatment purposes.
Why This Is Dangerous
An incorrect expiration date may lead to the use of a device that is no longer safe or effective. This poses significant health risks for patients relying on the device.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients may experience safety concerns and potential health risks from using the affected device. Immediate cessation of use is necessary to avoid harm.
Practical Guidance
How to identify if yours is affected
- Locate the model number and lot code on your LimFlow Vector device.
- Verify if the model is VT-US-23 and the lot code is 82321838.
- If your device matches, it is recalled.
Where to find product info
The model and lot number can typically be found on the device packaging or label.
What timeline to expect
Expect a response regarding refunds or replacements within 4-6 weeks after contacting LimFlow.
If the manufacturer is unresponsive
- Document all communications with LimFlow.
- Contact the FDA or your healthcare provider for further assistance.
- Consider filing a complaint with the CPSC.
How to prevent similar issues
- Always check expiration dates on medical devices before use.
- Stay informed about product recalls through reputable sources.
- Consult with healthcare professionals for device safety.
Documentation advice
Keep records of your purchase, communications with LimFlow, and any medical advice received.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
Product Details
The recalled product is the LimFlow Vector, model VT-US-23, with lot code 82321838. It was distributed nationwide in states including Alabama, California, New York, and Texas.
Key Facts
- Recalled model: LimFlow Vector VT-US-23
- Incorrect expiration date poses health risks
- 33 units recalled nationwide
- Patients should cease use immediately
Browse More Recalls
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.
