Medical device recalls Moderate risk

Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT SP - Model no. 728311 Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems…

Recall date
February 8, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1409-2018
FDA classification
Class II
Brand / firm
Philips Medical Systems (Cleveland) Inc
Sold / distributed
Worldwide Distribution - U.S. Nationwide. International distribution to Canada, Mexico, Algeria, Argentina, Australia, Austria, Bangladesh, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria, Cambodia, Chile, China, Colombia, Croatia, Cuba, Czech Republic, Denmark, Djibouti, Dominican Repub…

Why it was recalled

Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Brilliance iCT SP - Model no. 728311 Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories.

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