FDA Medical Device Recalls (openFDA)
Philips Medical Systems, Inc. Cardiac & Monitoring Systems: Viridia/Agilent Information Center Model : M3151A#CO1
- Recall number
- Z-0595-03
- Recalling firm
- Philips Medical Systems, Inc. Cardiac & Monitoring Systems
- Product
- Viridia/Agilent Information Center Model : M3151A#CO1
- Status
- Terminated
- Initiated
- 2003-01-02
- Posted
- 2003-02-28
- Terminated
- 2006-02-15
- Reason
- Central Station Monitoring Information Centers may experience sreeen freeze, i.e. loss of display, keyboard or mouse lock up
- Root cause
- Other
- Action
- Philips Medical Systems notified users by Certified Mail on/about 2/19/03 that the firm was initiating a device field correction (recall) to conduct an upgrade to units witha HP VL400 or VL420 computer which is cconfigured for dual display by replacing the video and network communication card. Previous to this notification, Philips sent letters on 1/2/03 addressed to Biomedical Engineering Manager to advise users to reboot the system in the event of a system freeze.
- Quantity
- 82 units
- Distribution
- Nationwide Canada, Europe, Asia, Latin America
- Lot, serial or model codes
- Serial# 4102A00874 4102A00889 4102A00890 4102A00894 4102A00905 4102A00920 4102A00945 4102A00957 4102A00971 4102A00972 4102A00984 4102A01011 4102A01029 4102A01030 4102A01031 4102A01032 4136A01100 4136A01101 4136A01102 4136A01103 4136A01104 4136A01105 4136A01106 4136A01116 4136A01117 4143A01190 4143A01191 4143A01192 4143A01213 4143A01227 4143A01244 4143A01289 4143A01290 4143A01291 4143A01292 4143A01311 4143A01312 4213A01338 4213A01345 4213A01346 4213A01383 4213A01386 4213A01398 4213A01399 4213A01400 4213A01401 4213A01402 4213A01403 4213A01404 4213A01405 4213A01406 4213A01407 4213A01412 4213A01416 4213A01420 4213A01421 4213A01425 4213A01442 4213A01452 4213A01468 4213A01472 4213A01479 4213A01481 4213A01482 4213A01483 4213A01484 4213A01485 4213A01486 4213A01490 4213A01491 4143A01175 4143A01249 4143A01250 4143A01251 4143A01252 4143A01253 4213A01347 4143A01178 4213A01469 4102A00903 4102A00904 4102A00892
- 510(k) numbers
- ["K011093"]
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 1218950
- Firm city
- Andover
- Firm state
- MA
- 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