FDA Medical Device Recalls (openFDA)
Philips Medical Systems: Philips BV300 Mobile X-Ray System
- Recall number
- Z-0526-03
- Recalling firm
- Philips Medical Systems
- Product
- Philips BV300 Mobile X-Ray System
- Status
- Terminated
- Initiated
- 2002-09-27
- Posted
- 2003-02-01
- Terminated
- 2005-01-12
- Reason
- The C-bow support can bend and break allowing C-arm to fall from support
- Root cause
- Other
- Action
- The firm issued a letter dated 9/27/02 to their customers. The letter advised of the problem and that a service representative will visit to inspect unit and correct.
- Quantity
- 229 devices
- Distribution
- The firm distributed to hospitals, x-ray centers and medical centers throughout the U.S.
- Lot, serial or model codes
- Part numbers 9896 000 06801 and 9806 000 06802 with serial numbers: DBXXXX - all DBXXXX - all DDXXXX - all DEXXXX - all DG0001-DG0129 DH0001-DH0033 DJ0001 - DJ0152 DK0001 - DK 0076
- 510(k) numbers
- ["K953910"]
- PMA numbers
- not on file
- Product code
- IZL
- 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