FDA recall Z-1582-2018

Radiometer Medical ApS · Class II · device

Product

AQURE, Software version 2.3.0 and 2.3.1 Product Usage: The AQURE system is intended to let allow the management of analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from connected devices at the point-of care or laboratory. It can send test results to the HIS/LIS. The system lets the user send commands to selected devices. The system uses data related to the performance of devices, to tell users of issues to be managed. The AQURE system is intended for professional use.

Reason for recall

There is a potential problem relating to the AQURE System, versions 2.3.0 and 2.3.1, that may result in patient mix-up.

Distribution

US Nationwide Distribution in the states to Georgia and Wisconsin.

Key facts

Status
Terminated
Initiation date
2018-02-27
Report date
2018-05-09
Termination date
2019-03-20
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bronshoj, N/A, Denmark

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1582-2018