ASTRA, LLC: Medical Device Recall in 2019 - (Recall #: Z-2100-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 25, 2019

Date Posted: August 14, 2019

Recall Number: Z-2100-2019

Event ID: 83302

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1 product

Code Information:

Model: L1, identified by Accession No. RH19A0069

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated