Recall Z-1218-2026— LimFlow, Inc.

Name: FDA recall Z-1218-2026
Creator: U.S. Food and Drug Administration
Published: 2025-12-05

Class II · Ongoing

Class II FDA medical device recall by LimFlow, Inc., initiated 2025-12-05. It names one FDA 510(k) clearance: K221902. Product: Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23. Reason: Incorrect expiration date.

Recalling firm: LimFlow, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-12-05
Firm location: San Jose, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K221902 — LimFlow VectorLimFlow, Inc.·cleared 2022-12-21

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

Reason for recall

Incorrect expiration date

Data sourced from openFDA. This site is unofficial and independent of the FDA.