Siemens Medical Solutions USA, Inc recalls MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light

Recalled December 19, 2012 · FDA recall Z-0515-2013 · Siemens Medical Solutions USA

Hazard

A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems. · FDA Class II

Units

1315

Sold at

Nationwide Distribution

Description

A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.

Product

MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light

Manufacturer(s)

Siemens Medical Solutions USA, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →