LimFlow recalled 33 units of its Vector model VT-US-23 on December 5, 2025, due to incorrect expiration dates. Patients and healthcare providers should stop using this device immediately. The recall affects distribution across 14 states and the District of Columbia.
Incorrect expiration date
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact LimFlow, Inc. or your healthcare provider for instructions. Notification method: Letter
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The LimFlow Vector is a medical device designed for specific healthcare applications. Patients and healthcare providers rely on its proper functionality for treatment purposes.
An incorrect expiration date may lead to the use of a device that is no longer safe or effective. This poses significant health risks for patients relying on the device.
This recall is not part of a broader industry pattern.
Patients may experience safety concerns and potential health risks from using the affected device. Immediate cessation of use is necessary to avoid harm.
The model and lot number can typically be found on the device packaging or label.
Expect a response regarding refunds or replacements within 4-6 weeks after contacting LimFlow.
Keep records of your purchase, communications with LimFlow, and any medical advice received.
The recalled product is the LimFlow Vector, model VT-US-23, with lot code 82321838. It was distributed nationwide in states including Alabama, California, New York, and Texas.
Not sure what to do next? Our guide walks you through the process step by step.
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