🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: April 25, 2019 ASTRA Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model: L1, identified by Accession No. RH19A0069
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
ASTRA, LLC
Reason for Recall:
Failure to comply event due to incorrect labeling of a class 1 laser product.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full 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 Codes/Lot Numbers:

Model: L1, identified by Accession No. RH19A0069

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2100-2019