Class 2 Device Recall

• Date Initiated by Firm: February 20, 2002
• Date Posted: September 12, 2003
• Recall Status: Terminated on April 11, 2005
• Recall Number: Z-1204-03
• Recall Event ID: 26581
• 510(K)Number: K912470
• Product Classification: Table, Radiographic, Non-Tilting, Powered - Product Code IZZ
• Product: Multidiagnost 96
• Code Information: The firm utilizes a site number specific to each unit: 17197, 17368, 17325, 76449, 17247, 17339, 17304, 13444, 6616, 6558, 6559, 6426, 6539, 6541, 6583, 35366, 37859, 31000, 67642, 62363, 62362, 62278, 62300, 25769, 25901, 25884, 25768, 25900, 25888, 25834, 25967, 25710, 25907, 62279, 62310, 62403, 62391, 62309, 62404, 73921, 50135, 44742, 44670, 44703, 44760, 44699, 46921, 52354
• FEI Number: 1000524572
• Recalling Firm/ Manufacturer: Philips Medical Systems; 22100 Bothell Everett Highway; Bothell WA 98041
• For Additional Information Contact: 425-487-7000
• Manufacturer Reason for Recall: Spontaneous movement of table without input from an operator
• FDA Determined Cause: Other
• Action: On 2/20/02 the firm issued Field Change Order to their field personnel, instructing them to visit each site and upgrade each unit.
• Quantity in Commerce: 48 units
• Distribution: The firm distributed units to hospitals and medical centers located throughout the US.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 �7.55.

• 510(K) Database: 510(K)s with Product Code = IZZ