FDA Medical Device Recalls (openFDA)
Philips Medical Systems Sales & Service Region No. America: Diagnost 96
- Recall number
- Z-1212-03
- Recalling firm
- Philips Medical Systems Sales & Service Region No. America
- Product
- Diagnost 96
- Status
- Terminated
- Initiated
- 2003-08-10
- Posted
- 2003-09-11
- Terminated
- 2005-01-13
- Reason
- Potential for table to move by itself
- 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
- 54
- Distribution
- The firm distributed devices to hospitals and medical centers located throughout the U.S.
- Lot, serial or model codes
- 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
- 510(k) numbers
- K912470
- PMA numbers
- not on file
- Product code
- IZZ
- Firm FEI
- 1000524572
- Firm city
- Bothell
- Firm state
- WA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28