Philips Healthcare Inc. recalls Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Pro

Recalled June 26, 2013 · FDA recall Z-1447-2013 · Philips Healthcare

Hazard

Installation Acceptance Test Document (IATD) non compliant with regulations IATDs (Installation Acceptance Test could not be located or different templates have been used · FDA Class II

Units

177 units

Sold at

Worldwide Distribution - USA Nationwide and the country of Canada

Description

Installation Acceptance Test Document (IATD) non compliant with regulations IATDs (Installation Acceptance Test could not be located or different templates have been used

Product

Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD Applications

Manufacturer(s)

Philips Healthcare Inc.

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