FDA recall, , Moderate risk
LimFlow Vector
The LimFlow Vector has an incorrect expiration date.
Summary by Recall Canary from the FDA notice
What happened
LimFlow, Inc., of San Jose, California, recalled the LimFlow Vector, model VT-US-23, because of an incorrect expiration date. The company began the recall on December 5, 2025, and the FDA added it to the Enforcement Report on January 29, 2026. The product was distributed in Alabama, Connecticut, the District of Columbia, Florida, Kentucky, Massachusetts, Michigan, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Texas, and Wyoming.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and lot code listed under your product.
LimFlow Vector
- Model number
- VT-US-23
- Lot code
- 82321838
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Alabama, Connecticut, District of Columbia, Florida, Kentucky, Massachusetts, Michigan, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Texas, Wyoming.
- Company
- LimFlow, Inc.San Jose, California
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98218
- Recall number
- Z-1218-2026
- Quantity recalled
- 33 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
