Device Recall: LimFlow Vector VT-US-23
Announced 2026-02-04 · FDA
The FDA notes a recall of 33 LimFlow Vector devices (Model VT-US-23) due to an incorrect expiration date. The affected devices were distributed nationwide across states AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY. The recall identifiers include Lot Code VT-US-23 Lot 82321838, GTIN 00850041730134, and U.S. Product Code MGZ; no corrective action is listed.
| Brand | LimFlow, Inc. |
|---|---|
| Product | Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23 |
| Reason | Incorrect expiration date |
| Severity | moderate |
| Units affected | 33 |
| 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. |
| Agency | FDA |
| Recall / campaign no. | Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ |
WHAT YOU SHOULD DO
- Verify whether you own a LimFlow Vector VT-US-23 device by checking the lot code 82321838, GTIN 00850041730134, and U.S. Product Code MGZ.
- If affected, stop using the device and contact LimFlow, Inc. or your healthcare provider for replacement, refund, or further instructions.
- Retain this recall notice and await further guidance from the manufacturer or FDA.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.