FDA Medical Device Recalls (openFDA)
Philips Medical Systems: EasyWeb
- Recall number
- Z-1128-03
- Recalling firm
- Philips Medical Systems
- Product
- EasyWeb
- Status
- Terminated
- Initiated
- 2002-02-13
- Posted
- 2003-08-12
- Terminated
- 2005-01-12
- Reason
- Potential for incorrect body part information
- Root cause
- Other
- Action
- A letter dated 2/13/02 was issued to customers advising that a representative from the firm will install new software.
- Quantity
- 28
- Distribution
- The firm distributed units to hospitals and medical centers located throughout the US.
- Lot, serial or model codes
- The firm assigns a ''site number'' to each device: Z1776, 86233, 86264, 83198, 86944, 85075, 85077, 85083, 85071, 85067, 10377, 85048, 86026, X1676, 83675, 86025, 87131, 87158, 82683, 84027, 84087, 84359, 86007, 84405, 85453, 83917, 85189, 83961
- 510(k) numbers
- ["K982769"]
- PMA numbers
- not on file
- Product code
- LLZ
- 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