Device Recall: LimFlow Vector VT-US-23
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 |
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.
How to identify the recalled item
| Lot / date codes | Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ |
|---|---|
| Lot / date codes | Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
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.