FDA Medical Device Recalls (openFDA)
Weber Marking System Inc.: Weber SolarJet S CO2 Vector Laser Coder System; Weber Marking Systems, Inc., Arlington Heights, IL 60005
- Recall number
- Z-0153-04
- Recalling firm
- Weber Marking System Inc.
- Product
- Weber SolarJet S CO2 Vector Laser Coder System; Weber Marking Systems, Inc., Arlington Heights, IL 60005
- Status
- Terminated
- Initiated
- 2003-09-12
- Posted
- 2004-07-20
- Terminated
- 2004-04-29
- Reason
- The laser product failed to comply with the performance standards, including certification, identification, warning logotype label, aperture label and submission of a product report.
- Root cause
- Other
- Action
- Recalled by letter dated 9/12/03. The user account was advised of the labeling non-compliances and that a Weber Marking Systems representative would visit their location to correct the laser unit.
- Quantity
- 1 unit
- Distribution
- Virginia
- Lot, serial or model codes
- serial number 09333451
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LS-99
- Firm FEI
- 1000298911
- Firm city
- Arlington Heights
- Firm state
- IL
- 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