Home / Recalls / Medical Devices
ASTRA, LLC recalls Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed abov
Recalled August 14, 2019 · FDA recall Z-2100-2019 · ASTRA
Hazard
Failure to comply event due to incorrect labeling of a class 1 laser product. · FDA Class II
Units
1 product
Sold at
US Nationwide Distribution
Description
Failure to comply event due to incorrect labeling of a class 1 laser product.
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
Manufacturer(s)
ASTRA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →