FDA Medical devices recall ·
LimFlow Vector Product Name: LimFlow Vector Model recall
- Recall number
- Z-1218-2026
- Date
- (initiated December 5, 2025)
- Company / brand
- LimFlow, Inc.
3031 Tisch Way Ste 110, San Jose, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 33 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Why was it recalled?
Incorrect expiration date
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ
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.
States: Alabama Connecticut District of Columbia Florida Kentucky Massachusetts Michigan Nebraska New Jersey New York Ohio Pennsylvania Rhode Island Texas Wyoming
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1218-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.