Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Summary
The FDA issued a Class II for Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: by LimFlow, Inc.. Reason: Incorrect expiration date.
Details
Source
Device Recall
External ID
Z-1218-2026
Action Date
2026-02-04
Status
Ongoing
Category
device
Product Description
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Lot/Code Info: Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ
Quantity Affected: 33 units
Reason for Recall
Incorrect expiration date
Distribution
US Nationwide distribution in the states of AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-05
Company
San Jose, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 175 device recalls issued in the same week, part of 403 device-related FDA actions this month.
LimFlow, Inc. has 7 FDA actions in our database, including 1 recall and 6 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (LimFlow, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LimFlow, Inc. have FDA actions?
LimFlow, Inc. has 7 FDA actions in our database, including 1 recall and 6 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1218-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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