Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have a malfunction where they...

Date: November 15, 2024
Company: Mint Medical GmbH
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Mint Medical GmbH directly.

Affected Products

mint Lesion, Software Versions: 3.10.0 and 3.10.1.

Quantity: 18 units (7 US, 11 OUS)

Why Was This Recalled?

Some software versions have a malfunction where they may show incorrect orientation labels for a specific subset of DICOM images.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Mint Medical GmbH

Mint Medical GmbH has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report