FDA Medical Device Recalls (openFDA)
Philips Medical Systems Sales & Service Region No. America: Diagnost 94
- Recall number
- Z-1214-03
- Recalling firm
- Philips Medical Systems Sales & Service Region No. America
- Product
- Diagnost 94
- 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
- see Diagnost 96 above
- Distribution
- The firm distributed devices to hospitals and medical centers located throughout the U.S.
- Lot, serial or model codes
- See Diagnost 96 above
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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