FDA Medical Device Recalls (openFDA)
Philips Medical Systems: Multidiagnost 96
- Recall number
- Z-1204-03
- Recalling firm
- Philips Medical Systems
- Product
- Multidiagnost 96
- Status
- Terminated
- Initiated
- 2002-02-20
- Posted
- 2003-09-12
- Terminated
- 2005-04-11
- Reason
- Spontaneous movement of table without input from an operator
- 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
- 48 units
- Distribution
- The firm distributed units to hospitals and medical centers located throughout the US.
- Lot, serial or model codes
- 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
- 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