Z-1212-03

Diagnost 96

Name: Z-1212-03 Diagnost 96
Creator: Philips Medical Systems Sales & Service Region No. America
Published: 2003-08-10
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2003-08-10 / Terminated

FDA source

Philips Medical Systems Sales & Service Region No. America began a recall of Diagnost 96 on 2003-08-10. The reason FDA records is "Potential for table to move by itself". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1212-03
Status: Terminated
Initiated: 2003-08-10
Posted: 2003-09-11
Terminated: 2005-01-13
Recalling firm: Philips North America LLC
Product: Diagnost 96
Product code: IZZ Table, Radiographic, Non-Tilting, Powered
Reason for recall: Potential for table to move by itself
FDA root cause: Other
Action: The firm issued a letter dated 8/10/03 informing the consignees of the error and advising that a service employee will be visiting each site for software upgrade.
Quantity in commerce: 54
Distribution: The firm distributed devices to hospitals and medical centers located throughout the U.S.
Product codes and lots: Part Number: 9804 405 80001, 9804 405 80101, 9896 000 1284, 9896 000 12851, 9896 000 12451, 9896 000 1262, 9896 000 59041 The firm utilizes a site number specific to each unit: 6993, 62309, 25710, 25901, 62279, 13709, 62635, 76345, 41372, 31000, 17197, 25900, 62300, X0668, 13444, 6981, 6559, 6426, 6583, 38530, 6852, 683, 25907, 44760, 44670, 17368, 17325, 25769, 13951, 13608, 17247, 38507, 26018, 62278, 62391, 17304, 46921, 45014, 45013, 67642, 62404 37859, 86113, 38023, 6541, 74057, 74056, 61667, 62666, 62403, 62310, 35366, 50135, 13971, 25768, 62988, 62885, 38897, 6558, 44699, 76449, 25967, 25884, 25834, 44742, 6935, 40940, 62363, 62362, 38500, X1207, 6539, X1069, 6616, 17436, 59633, 52354, 47166, 17605, 17339, 62504, 62937, 62936, 59497

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)