LimFlow Vector Devices Recalled for Incorrect Expiration Date

Agency Publication Date: January 29, 2026

Summary

LimFlow, Inc. is recalling 33 units of the LimFlow Vector (Model VT-US-23) because the product labels list an incorrect expiration date. Using a medical device past its intended shelf life can compromise its performance or sterility. Consumers and healthcare facilities should identify the affected lot to ensure expired products are not used in clinical procedures.

Risk

The incorrect expiration date may lead healthcare providers to use the device after its validated shelf life, potentially resulting in device failure or increased risk of infection if the sterile barrier has degraded.

What You Should Do

Check your inventory for the LimFlow Vector, Model VT-US-23, specifically Lot number 82321838.
Verify the GTIN (00850041730134) and U.S. Product Code (MGZ) on the packaging to confirm if your device is affected.
Stop using the recalled device immediately.
Contact LimFlow, Inc. or your distributor to arrange for the return, replacement, or correction of the affected units.
Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.

Your Remedy Options

Other Action

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: LimFlow Vector

Model / REF:

VT-US-23

Lot Numbers:

82321838

GTIN:

00850041730134

U.S. Product Code: MGZ; Recall #: Z-1218-2026

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 98218

Status: Active

Manufacturer: LimFlow, Inc.

Sold By: Direct distribution to hospitals and clinics

Manufactured In: United States

Units Affected: 33 units

Distributed To: Alabama, Connecticut, District of Columbia, Florida, Kentucky, Massachusetts, Michigan, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Texas, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

Check your inventory for the LimFlow Vector, Model VT-US-23, specifically Lot number 82321838.

Verify the GTIN (00850041730134) and U.S. Product Code (MGZ) on the packaging to confirm if your device is affected.

Stop using the recalled device immediately.

Contact LimFlow, Inc. or your distributor to arrange for the return, replacement, or correction of the affected units.

Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.