FDA recall Z-2100-2019

Product

Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access

Reason for recall

Failure to comply event due to incorrect labeling of a class 1 laser product.

Distribution

US Nationwide Distribution

Key facts

Status

Ongoing

Initiation date

2019-04-25

Report date

2019-08-14

Voluntary/Mandated

FDA Mandated

Location

Louisville, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2100-2019