Z-1204-03

Multidiagnost 96

Name: Z-1204-03 Multidiagnost 96
Creator: Philips Medical Systems
Published: 2002-02-20
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2002-02-20 / Terminated

FDA source

Philips Medical Systems began a recall of Multidiagnost 96 on 2002-02-20. The reason FDA records is "Spontaneous movement of table without input from an operator". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1204-03
Status: Terminated
Initiated: 2002-02-20
Posted: 2003-09-12
Terminated: 2005-04-11
Recalling firm: Philips North America LLC
Product: Multidiagnost 96
Product code: IZZ Table, Radiographic, Non-Tilting, Powered
Reason for recall: Spontaneous movement of table without input from an operator
FDA root 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.
Product codes and lots: 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

Product code IZZ

K912470Class IIPhilips Diagnost 96Philips Medical Systems, Inc. / cleared 1991-08-07

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)