FDA Medical Device Recalls (openFDA)
Trimble Ab: The Trimble RTS873 robotic total station is a solution designed for construction professionals seeking precision, efficiency, and reliability in their layout tasks. The integrated Class 2 green aiming laser system enhances visibility and accuracy, even on uneven surfaces. It is ideal for general and specialty contractors, the RTS873 streamlines layout processes, reduces rework, and enhances overall productivity.
- Recall number
- Z-1661-2025
- Recalling firm
- Trimble Ab
- Product
- The Trimble RTS873 robotic total station is a solution designed for construction professionals seeking precision, efficiency, and reliability in their layout tasks. The integrated Class 2 green aiming laser system enhances visibility and accuracy, even on uneven surfaces. It is ideal for general and specialty contractors, the RTS873 streamlines layout processes, reduces rework, and enhances overall productivity.
- Status
- Open, Classified
- Initiated
- 2025-03-26
- Posted
- 2025-04-28
- Terminated
- not on file
- Reason
- An issue has been identified in the production of the RTS873 robotic total stations that may result in the green aiming laser output power being above its laser safety Class 2 classification.
- Root cause
- Under Investigation by firm
- Action
- Product Bulletin sent 03/05/2025. Customers sold affected products have been notified by Trimble and are currently in the process of contacting end customers and informing them of the up-coming service of their products.
- Quantity
- 127
- Distribution
- US and OUS (South Korea and United Kingdom).
- Lot, serial or model codes
- Trimble RTS873 instruments produced from October 2023 to February 12, 2025.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- REP
- Firm FEI
- 3003881956
- Firm city
- Danderyd
- Firm state
- not on file
- Firm country
- Sweden
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