ASTRA, LLC 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
ASTRA, LLC
Lot Codes / Batch Numbers
Model: L1, identified by Accession No. RH19A0069
Products Sold
Model: L1, identified by Accession No. RH19A0069
ASTRA, LLC is recalling Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is inst due to Failure to comply event due to incorrect labeling of a class 1 laser product.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to comply event due to incorrect labeling of a class 1 laser product.
Recommended Action
Per FDA guidance
Corrected labels have been applied to the installed product as of May 6, 2019. Additionally, all corresponding documentation provided to customer (users manual) has been updated to reflect the updated label. The correction implemented at no cost to the purchaser
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026