Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Compu...

FDA Recall #Z-2709-2014 — Class II — December 27, 2005

Recall #Z-2709-2014 Date: December 27, 2005 Classification: Class II Status: Terminated

Product Description

Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Computed tomography scanner intended to provide cross sectional images of the human body and visualization of the internal organs.

Reason for Recall

The system has a gap that can appear between the upper and lower tilt stand covers. The fingers may be squeezed if a person was to place them in this region while the gantry was tilting from an angle to zero tilt angle.

Recalling Firm

Philips Medical Systems (Cleveland) Inc — Cleveland, OH

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

364

Distribution

Worldwide Distribution -- AZ, CO, GA, IA, IL, IN, KS, KY, MD, MI, MN, MS, NC, NY, OH, OK, TX, VT, and WI; and, countries of Singapore, New Zealand, India, Australia, Korea, Japan, Korea, China, India, Taiwan, Australia, Turkey, France, South Africa, Spain, Italy, Austria, Belgium, Switzerland, Israel, Netherlands, England, and Brazil.

Code Information

728256, 728251, 728246, 728240, and 728235.

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated