FDA-Device2026-02-04Class IIMISBRANDING
LimFlow Vector vascular device recalled for incorrect expiration date
What this means
LimFlow Vector vascular devices (Model VT-US-23, Lot 82321838) were distributed with an incorrect expiration date printed on the packaging. This affects 33 units distributed across multiple U.S. states. An incorrect expiration date could lead to use of a device beyond its safe lifespan.
- Check any LimFlow Vector devices in your care for Lot 82321838
- Verify the printed expiration date and do not use if it appears incorrect
- Contact your hospital or facility's medical device coordinator or LimFlow, Inc. for instructions
- Report any issues or use of affected devices to the FDA's MedWatch program
The agency's original wording
Hazard
Incorrect expiration date
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the states of AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY.
Affected count
33 units
Manufactured in
3031 Tisch Way Ste 110, N/A, San Jose, CA, United States
Products
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1218-2026Want us to check the next one for you?
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