Cellavision AB: Medical Device Recalls in 2018

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Cellavision AB in 2018. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the following products: CellaVision DM96, DM1200, DM9600 and DI-60 Product Usage: The devices are automated cell-locating devices. The devices automatically locates and presents images of blood cells on peripheral blood smears. The operator identifies and verifies the suggested classification of each cell according to type. The devices are intended to be used by skilled operators, trained in the use of the device and in recognition of blood cells