United StatesMint Lesion software (versions 3.4.0 through 3.9.5; UDI‑DI: 04260495880341, 04260495880358, 04260495880365, 04260495880372, 04260495880389, 04260495880396), installed on 101 systems and distributed worldwide, is being recalled by Mint Medical GmbH. If the connection between a Mint Lesion workstation and the Mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.
What's being recalled
Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.;
Recalling firm: Mint Medical GmbH, Dossenheim, Germany.
How to identify it
Software Versions: 3.4.0 up to 3.9.5. UDI-DI: 04260495880341, 04260495880358, 04260495880365, 04260495880372, 04260495880389, 04260495880396.
The hazard
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide distribution - US Nationwide and the countries of Germany, Switzerland, Austria, Belgium, Italy, France, Romania, Netherlands, United Kingdom, Spain, Czech Republic, Ireland, Poland;
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)