The Trimble RTS873 robotic total station is a solution designed for construction professionals seeking precision, effici
Summary
The FDA issued a Class II for The Trimble RTS873 robotic total station is a solution designed for construction by Trimble Ab. 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.
Details
Source
Device Recall
External ID
Z-1661-2025
Action Date
2025-05-07
Status
Ongoing
Category
device
Product Description
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.
Lot/Code Info: Trimble RTS873 instruments produced from October 2023 to February 12, 2025.
Quantity Affected: 127
Reason for Recall
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.
Distribution
US and OUS (South Korea and United Kingdom).
Type: FDA Mandated
Recall Initiated: 2025-03-26
Company
Danderyd
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 149 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Trimble Ab) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Trimble Ab have FDA actions?
This is the only FDA action we have on record for Trimble Ab in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1661-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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